Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Parke-Davis Co. — Predicate Candidate Screening
47 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
51 daysmedian FDA review time
165 days90th percentile
47clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K861725 | INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT | Parke-Davis Co. | 1986-12-04 | 212 | 0 |
| K862119 | DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR | Parke-Davis Co. | 1986-08-29 | 87 | 0 |
| K855120 | ATI DISPOSABLE BIOLOGICAL TEST PACK | Parke-Davis Co. | 1986-06-18 | 177 | 0 |
| K860570 | ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE | Parke-Davis Co. | 1986-03-31 | 45 | 0 |
| K860290 | VIAPIC CENTRAL LINE CATHETER | Parke-Davis Co. | 1986-03-18 | 49 | 0 |
| K852192 | DISPOSABLE STEAM BIOLOGICAL TEST PACK | Parke-Davis Co. | 1985-11-01 | 165 | 0 |
| K841967 | DESERET THERMODILUTION CARDIAC OUTPUT | Parke-Davis Co. | 1985-08-19 | 461 | 0 |
| K851327 | DESERET ARTERIAL CATHETER | Parke-Davis Co. | 1985-06-14 | 71 | 0 |
| K852078 | SPECTRUM(TENTATIVE) | Parke-Davis Co. | 1985-06-07 | 25 | 0 |
| K844840 | DESERET INTRODUCER SET | Parke-Davis Co. | 1985-05-16 | 155 | 0 |
| K850505 | DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER | Parke-Davis Co. | 1985-03-11 | 31 | 2 |
| K850439 | DESERET EPIDURAL CATHETER | Parke-Davis Co. | 1985-03-05 | 28 | 0 |
| K843033 | DESERET INTRAVASCULAR CATHETER | Parke-Davis Co. | 1984-12-03 | 124 | 0 |
| K844113 | DESERET SUBCLAVIAN JUGULAR CATHETER SET | Parke-Davis Co. | 1984-11-28 | 36 | 0 |
| K844219 | DESERET DENTRAL LINE CATHETER | Parke-Davis Co. | 1984-11-28 | 28 | 0 |
| K841968 | DESERET DISPOSABLE PRESSURE TRANSDUCER | Parke-Davis Co. | 1984-08-06 | 83 | 0 |
| K841317 | DESERET HEPARIN COATED FLOW DIRECTED | Parke-Davis Co. | 1984-06-11 | 70 | 0 |
| K841251 | DESERET HEPARIN COATED FLOW CATH | Parke-Davis Co. | 1984-06-11 | 77 | 0 |
| K841168 | STERILIZATION PROCESS INDICATOR | Parke-Davis Co. | 1984-05-09 | 51 | 0 |
| K840958 | DESERET LONG TERM INDWELLING CATHETER | Parke-Davis Co. | 1984-04-17 | 42 | 0 |
| K840116 | DESERET INFANT CENTRAL VENOUS CATHE- | Parke-Davis Co. | 1984-03-22 | 71 | 0 |
| K840355 | DESERET MULTILUMEN SUBCLAVIAN JUGULAR | Parke-Davis Co. | 1984-03-19 | 53 | 0 |
| K840183 | DESERET MULTILUMEN SUBCLAVIAN JUGULAR | Parke-Davis Co. | 1984-03-19 | 62 | 0 |
| K840862 | DESERET CENTRAL VENOUS CATHETER | Parke-Davis Co. | 1984-03-19 | 24 | 0 |
| K834227 | DESERET SUBCLAVIAN JUGULAR CATH. SET | Parke-Davis Co. | 1984-03-19 | 104 | 0 |
| K834393 | DESERET NEONATAL CATHETER SET | Parke-Davis Co. | 1984-02-13 | 61 | 0 |
| K833976 | VANISH | Parke-Davis Co. | 1984-02-04 | 79 | 0 |
| K834472 | DESERET EPIDURAL CATHETER | Parke-Davis Co. | 1984-01-13 | 24 | 0 |
| K832352 | 3-DAY RELEASE OF ETHYLENE OXIDE DEVICE | Parke-Davis Co. | 1984-01-13 | 182 | 0 |
| K833135 | INTRACATH INTRAVENOUS CATHETER UNIT | Parke-Davis Co. | 1983-11-21 | 68 | 0 |
| K832058 | ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV. | Parke-Davis Co. | 1983-09-12 | 77 | 0 |
| K823064 | INTRACATH-DA INTRAVENOUS CATH. PLACEMENT | Parke-Davis Co. | 1983-01-27 | 101 | 0 |
| K823086 | DESERET SURGEON'S GLOVE ACCESSORY | Parke-Davis Co. | 1983-01-17 | 90 | 0 |
| K823065 | INTRA CATH-DSA INTRAVENOUS CATH PLACE. | Parke-Davis Co. | 1982-12-15 | 58 | 0 |
| K823066 | DESERT INSYTE-A HYPERTHERMIA SENSOR ACC | Parke-Davis Co. | 1982-11-17 | 30 | 0 |
| K782148 | HR UNIT | Parke-Davis Co. | 1979-01-08 | 17 | 0 |
| K781031 | AEROPLAST DRESSING | Parke-Davis Co. | 1978-07-27 | 38 | 0 |
| K771036 | SHAVE PREP TRAY | Parke-Davis Co. | 1977-07-14 | 34 | 0 |
| K770466 | STOCKINGS, RVS TM | Parke-Davis Co. | 1977-03-28 | 18 | 0 |
| K761035 | SURGICAL BLADE HANDLES | Parke-Davis Co. | 1976-12-21 | 36 | 0 |
| K760924 | TUCKS POLYPAD MATERNITY CARE PAD | Parke-Davis Co. | 1976-11-11 | 14 | 0 |
| K760817 | ORTHOPEDIC TUBULAR STOCKINETTE | Parke-Davis Co. | 1976-10-20 | 8 | 0 |
| K760578 | BALANCED CAST SOLE | Parke-Davis Co. | 1976-09-27 | 24 | 0 |
| K760342 | RAZOR, SCHICK DISPOSABLE | Parke-Davis Co. | 1976-08-11 | 12 | 0 |
| K760164 | UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX) | Parke-Davis Co. | 1976-07-20 | 14 | 0 |
| K760016 | SURGICAL BLADES (BEAVER) | Parke-Davis Co. | 1976-07-16 | 35 | 0 |
| K760113 | SPONGE, LAPAROTOMY GAUZE | Parke-Davis Co. | 1976-07-15 | 21 | 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