Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account
Warner-Lambert Co. — Predicate Candidate Screening
50 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
41 daysmedian FDA review time
93 days90th percentile
50clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K024160 | NEOSPORIN SCAR SOLUTION | Warner-Lambert Co. | 2003-03-17 | 90 | 0 |
| K893452 | EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAM | Warner-Lambert Co. | 1989-06-22 | 50 | 0 |
| K870584 | O.P.T.(TM) OVULATION PREDICTION TEST | Warner-Lambert Co. | 1987-11-25 | 287 | 0 |
| K861510 | MULTILUMEN VIAPIC CENTRAL LINE CATHETER | Warner-Lambert Co. | 1986-06-09 | 47 | 0 |
| K852967 | GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISK | Warner-Lambert Co. | 1985-08-19 | 35 | 0 |
| K852689 | GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK | Warner-Lambert Co. | 1985-08-19 | 55 | 0 |
| K852843 | GENERAL DIAGNOSTICS COAG-A-MATE XC | Warner-Lambert Co. | 1985-08-13 | 39 | 0 |
| K852889 | GENERAL DIAGNOSTICS RAPID E. COLI TEST | Warner-Lambert Co. | 1985-07-23 | 14 | 0 |
| K850410 | GEN. DIAG. CHROMOSTRATE PLASMINOGEN ASSAY | Warner-Lambert Co. | 1985-05-08 | 93 | 0 |
| K850486 | GENERAL DIAG. CHROMOSTRATE HEPARIN ASSAY | Warner-Lambert Co. | 1985-05-08 | 90 | 0 |
| K850409 | GEN. DIAG. CHROMOSTRATE REF. PLASMA | Warner-Lambert Co. | 1985-05-08 | 93 | 0 |
| K850411 | GEN. DIAG. CHROMOSTRATE ALPHA-2 ANTIPLASMIN ASSAY | Warner-Lambert Co. | 1985-05-08 | 93 | 0 |
| K850412 | GEN. DIAG. CHROMOSTRATE ANTITHROMBIN III ASSAY | Warner-Lambert Co. | 1985-05-08 | 93 | 0 |
| K850957 | GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK | Warner-Lambert Co. | 1985-05-01 | 54 | 0 |
| K851228 | GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISK | Warner-Lambert Co. | 1985-04-24 | 29 | 0 |
| K833369 | EARLY DETECTOR | Warner-Lambert Co. | 1984-08-02 | 310 | 0 |
| K833093 | VANISH II | Warner-Lambert Co. | 1983-12-12 | 91 | 0 |
| K833092 | DESERET ANGIO-GUIDE LARGE VEIN CATH. | Warner-Lambert Co. | 1983-11-21 | 70 | 0 |
| K833091 | DESERET SUBCLAVIAN JUGULAR CATH-SET | Warner-Lambert Co. | 1983-11-21 | 70 | 0 |
| K833352 | GEN. DIAGNOSTICS LOW FIBRINOGEN CONTROL | Warner-Lambert Co. | 1983-11-03 | 36 | 0 |
| K832599 | EARLY IN HOME PREGNANCY TEST | Warner-Lambert Co. | 1983-09-20 | 49 | 0 |
| K831535 | E.P.T. PLUS TM | Warner-Lambert Co. | 1983-06-30 | 48 | 0 |
| K830593 | ENSURE DRESSING | Warner-Lambert Co. | 1983-04-06 | 41 | 0 |
| K822991 | AO DOCUSTAR(MMIRO) FUNDUS CAMERA | Warner-Lambert Co. | 1983-02-24 | 135 | 0 |
| K822248 | DESERET ARTERIAL BLOOD SAMPLING KIT | Warner-Lambert Co. | 1982-10-21 | 84 | 0 |
| K822023 | DESERET SUBCLAVIAN JUGULAR CATH. SET | Warner-Lambert Co. | 1982-07-28 | 19 | 0 |
| K821886 | DESERET INSYTE HYPERTHERMIA CATHETER | Warner-Lambert Co. | 1982-07-28 | 33 | 0 |
| K821356 | DESERET CAPACITY PLUS ELECTROSURG. PAD | Warner-Lambert Co. | 1982-07-14 | 69 | 0 |
| K821865 | A O MICROSCOPE VIDEO SYSTEM | Warner-Lambert Co. | 1982-07-14 | 20 | 0 |
| K821831 | A O HISTOSTAT EMBEDDING CTR #8030,32,34 | Warner-Lambert Co. | 1982-07-13 | 21 | 0 |
| K821750 | DESERET E-Z SET INFUSION SET | Warner-Lambert Co. | 1982-07-02 | 17 | 0 |
| K821699 | DESERET SUBCLAVIAN JUGULAR CATHETER SET | Warner-Lambert Co. | 1982-06-24 | 16 | 0 |
| K821754 | A O FIBER OPTIC ILLUMINATOR, 1185B | Warner-Lambert Co. | 1982-06-24 | 9 | 0 |
| K821753 | A O FIBER OPTIC ILLUMINATION, 1185A | Warner-Lambert Co. | 1982-06-24 | 9 | 0 |
| K821525 | DESERET UNIVERSAL LUER LOCK | Warner-Lambert Co. | 1982-06-23 | 33 | 0 |
| K821577 | DESERET ANGIO GUIDE | Warner-Lambert Co. | 1982-06-16 | 19 | 0 |
| K821371 | DESERET SUBCLAVIAN JUGULAR CATHETER SET | Warner-Lambert Co. | 1982-06-02 | 23 | 0 |
| K821372 | DESERET INTRACATH INTRAVENOUS CATHETER | Warner-Lambert Co. | 1982-06-02 | 23 | 0 |
| K821245 | DESERET OFFSET PRN ADAPTER | Warner-Lambert Co. | 1982-05-13 | 14 | 0 |
| K813088 | DESERET NEOLON SURGICAL GLOVES | Warner-Lambert Co. | 1981-12-14 | 42 | 0 |
| K812073 | DESERET CATHETER DRESSING | Warner-Lambert Co. | 1981-10-06 | 77 | 0 |
| K812080 | AEGIS I.V. STRIPS | Warner-Lambert Co. | 1981-08-03 | 12 | 0 |
| K801538 | ASSURE LEVEL I PROD. #30171 | Warner-Lambert Co. | 1980-09-09 | 68 | 0 |
| K801539 | ASSURE LEVEL II PROD. #30172 | Warner-Lambert Co. | 1980-09-09 | 68 | 0 |
| K801335 | UNASSAYED CHEMISTRY SERUM CONTROL(BOVINE | Warner-Lambert Co. | 1980-07-08 | 34 | 0 |
| K801353 | PARKE-DAVIS SURGICAL LIGHT | Warner-Lambert Co. | 1980-06-30 | 21 | 0 |
| K801050 | SUPRA SCOPE | Warner-Lambert Co. | 1980-05-14 | 9 | 0 |
| K800363 | PARKE-DAVIS TOTAL KNEE PROSTHESIS | Warner-Lambert Co. | 1980-03-10 | 19 | 0 |
| K800118 | CHICK SURGICAL TABLE | Warner-Lambert Co. | 1980-02-05 | 18 | 0 |
| K791875 | PARKE-DAVIS TOTAL HIP PROSTHESIS | Warner-Lambert Co. | 1979-10-04 | 13 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda