Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

JJG — Predicate Candidate Screening

30 FDA 510(k) clearances under this product code; the 50 most recent screened below.

47 daysmedian FDA review time
104 days90th percentile
30clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K972409AG CHEMISTRY ANALYZER SYSTEMLandmark Scientific, Inc.1997-08-28630
K942782PICCOLO(TM)Abaxis, Inc.1995-03-132731
K934592EPOC 2000 POINT-OF-CARE ANALYZER AND EPOC 5-CHEMISTRY REAGENAbaxis, Inc.1994-04-061940
K920942OLYMPUS AU800 CLINICAL CHEMISTRY ANALYZEROlympus Corp.1992-06-101040
K910222COBAS ALPHARoche Diagnostic Systems, Inc.1991-02-27400
K903626BIOMEK AUTOMATED LABORATORY WORKSTATION W/GENELISABeckman Instruments, Inc.1990-10-15660
K893854COBAS FARA II CENTRIFUGAL ANALYZERRoche Diagnostic Systems, Inc.1989-08-03700
K893641COBAS FARA CENTRIFUGAL ANALYZERRoche Diagnostic Systems, Inc.1989-07-20660
K885203TECHNICON DAX(TM) SYSTEMTechnicon Instruments Corp.1989-03-28990
K871973IL MONARCH 1000 CLINICAL CHEMISTRY ANALYTICAL SYS.Instrumentation Laboratory CO1987-06-11200
K871838BIOMEK 1000C AUTOMATED LABORATORY WORK STATIONBeckman Instruments, Inc.1987-05-26140
K854523ANALYST PHYSICIAN'S OFFICE PROFILERE.I. Dupont DE Nemours & Co., Inc.1986-01-08570
K854055I.C.L.S. COMPULYZERIntegrated Computerized Laboratory Systems, Inc.1985-11-19470
K851619GEN PROFILER SYSTEMElectro-Cucleonics, Inc.1985-05-14260
K843914COBAS FLUORESCENCE POLARIZATION MODULERoche Diagnostic Systems, Inc.1984-11-27540
K842522PDA SYSTEMAbbott Laboratories1984-08-02360
K840231DISPOSABLE CUVETTE ARRAYConsumable Lab Supplies1984-03-22620
K832716ENCORE CHEMISTRY ANALYZERBaker Instructions Corp.1983-10-04530
K831571ROTORAmerican Scientific Products1983-06-30450
K831569REAGENT CUPSAmerican Scientific Products1983-06-30450
K830641ENCORE CHEMISTRY ANALYZERBaker Instructions Corp.1983-04-05350
K811525FLEXIGRAM AUTO LOADER SYSTEMElectro-Nucleonics Laboratories, Inc.1981-06-18200
K801139CENTRIFICHEM SYSTEM 500 ANALYZERUnion Carbide Corp.1980-06-09270
K801026IL MODEL 773 FLUORESCENCE LIGHT SCATTERInstrumentation Laboratory CO1980-05-28270
K792671COBAS-BIO CENTRIFUGAL ANALYZERHoffmann-La Roche, Inc.1980-01-17210
K791180CENTRIFICHEM SYSTEM 500Union Carbide Corp.1979-08-10460
K790550CENTRIA SYSTEMUnion Carbide Corp.1979-05-07480
K790278ANALYZER, CENTRIFUCHEM SYSTEM 400Union Carbide Corp.1979-04-04540
K781900ANALYZER, AUTOMED CENTRIFUGALAutogenic Systems1978-12-20370
K771813CENTRIFICHEM SYS 400 ANALYZERClinical Diagnostics, Inc.1977-10-25280

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