Atlas FDA

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

JLS — Predicate Candidate Screening

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

46 daysmedian FDA review time
126 days90th percentile
57clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K040923LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONIbl GmbH2004-07-221050
K973898PROGESTERONE ELISAKmi Diagnostics, Inc.1997-11-13300
K972133VITROS IMMUNODIAGNOSTICS PRODUCTS PROGESTERONE REAGENT PACK Johnson & Johnson Clinical Diagnostics, Inc.1997-06-24180
K971725OPUS PROGESTERONEBehring Diagnostics, Inc.1997-06-18400
K964841ELECSYS PROGESTERONE ASSAYBoehringer Mannheim Corp.1997-03-241110
K965084VIDAS PROESTERONE (PRG) (30 409)bioMerieux, Inc.1997-01-09210
K955025AXSYM PROGESTERONEAbbott Laboratories1996-03-071260
K955769ACCESS PROGESTERONE ASSAYBio-Rad Laboratories, Inc.1996-02-05462
K952075PROGESTERONE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-BITRBayer Corp.1995-06-13410
K951630AURAFLEX PROGESTERONE 150TEST PACKOrganon Teknika Corp.1995-05-08310
K950570STRATUS PROGESTERONE FLUOROMETRIC ENZYME IMMUNOASSAYBaxter Diagnostics, Inc.1995-04-11670
K944211IMMULITE PROGESTERONEDiagnostic Products Corp.1994-12-191121
K935138IMMULITE PROGESTERONEDiagnostic Products Corp.1994-01-11750
K933128SYNELISA PROGESTERONEElias U.S.A., Inc.1993-11-051300
K933269AIA-PACK(R) PROG ASSAYTosoh Medics, Inc.1993-10-221080
K931228PROGESTERONE RADIOIMMUNOASSAY KITImmunotech Corp.1993-10-222260
K933635STRATUS PROGESTERONE FLOUROMETRIC IMMUNOASSAYBaxter Diagnostics, Inc.1993-10-08730
K932955CIBA CORNING ACS PROGESTERONE IMMUNOASSAYCiba Corning Diagnostics Corp.1993-08-02467
K923410FIAGEN PROGESTERONECyberfluor, Inc.1992-12-031460
K920230AFFINITY PRGBd Becton Dickinson Vacutainer Systems Preanalytic1992-02-18320
K914462SRI PROGESTERONE ENZYME IMMUNOASSAY(MAG SOLD PHAS)Serono-Baker Diagnostics, Inc.1991-10-23160
K911512MILENIA PROGESTERONEDiagnostic Products Corp.1991-05-22480
K910683ENZYMUN-TEST PROGESTERONEBoehringer Mannheim Corp.1991-04-08480
K894049IMMUNOCOAT PROGESTERONE RADIOIMMUNOASSAY KITPantex, Div. Bio-Analysis, Inc.1989-09-08930
K890836RIA-GNOST PROGESTERONECambridge Medical Technology1989-03-16230
K890428DELFIA PROGESTERONE KITPharmacia, Inc.1989-02-23280
K884794PROGESTERONE SEROZYME IMMUNOENZYMETRIC ASSAYSerono-Baker Diagnostics, Inc.1989-02-02780
K884100AMERLITE PROGESTERONE ASSAY, LAN.0079/2079 240/144Amersham Corp.1988-11-10430
K880934MODIFIED AMERLEX-M PROGESTERONE RADIOIMMUNO. KITAmersham Corp.1988-04-18420
K873431PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PHSerono Diagnostics, Inc.1987-10-20550
K871211PROGESTERONE CLASP RADIOIMMUNOASSAY KITBiotecx Laboratories, Inc.1987-04-13180
K864855AMERLEX-M PROGESTERONE RADIOIMMUNOASSAY KITAmersham Corp.1987-02-25760
K864156PROGESTERONE SYSTEM BY EIAIntl. Bioclinical, Inc.1986-11-24320
K860924RAMP PROGESTURINE PDG ASSAY--48 TEST KITMonoclonal Antibodies, Inc.1986-07-021130
K854094IMMUCHEM COVALENT COAT A SOLID PHASE RADIOIMMUNOASImmuchem Corp.1986-02-281440
K854675DSL ANDROSTENEDIONE RIA (DSL #4200)Diagnostic Systems Laboratories, Inc.1986-01-28680
K854649DSL PROGESTERONE RIA (DSL #3400)Diagnostic Systems Laboratories, Inc.1985-12-13240
K850056LEECO PROGESTERONE-QUANT DIAGNOSTIC TEST KITLeeco Diagnostics, Inc.1985-02-06290
K845026AMERLEX-M PROGESTERONE RADIOIMMUNOASSAY KIT CODEAmersham Corp.1985-02-01360
K841333PROGESTERONE DIRECT RIA KIT-RADIOIMMBiotecx Laboratories, Inc.1984-05-02300
K840886HYDROXYPROGESTERONE BY RIA 17ARadioassay Systems Laboratories, Inc.1984-04-18510
K832694DIRIA-PROGK IMMUNOASSAYSorin Biomedica, Fiat, USA, Inc.1984-01-111540
K832297HYDROXYPROGESTERONE-17Diagnostics Biochem Canada, Inc.1983-09-01500
K830880IMMO PHASE DIRECT PROGESTERONE RADIO-Corning Medical & Scientific1983-04-18310
K820686LIQUISOL PROGESTERONE RADIOIMMUNODamon Corp.1982-04-01210
K820534COAT-A-COUNT PROGESTERONE KIA KITDiagnostic Products Corp.1982-03-16140
K813484PROGESTERONE KIT BY RIAImmuchem Corp.1981-12-22210
K811907PROGESTERONE DIRECT RIA KIT (125I)Immunalysis Corporation1981-07-23220
K811369NATAL-TEC PROGESTERONEArmkel, LLC1981-05-29150
K810804PROGESTERONE KITCambridge Nuclear Corp.1981-04-0180

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