Atlas FDA

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

GIM — Predicate Candidate Screening

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

57 daysmedian FDA review time
259 days90th percentile
39clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K240455BD Vacutainer® Citrate Blood Collection TubesBecton, Dickinson and Company2024-10-312590
K230493BD MiniDraw Capillary Blood Collection System with BD MiniDrBecton, Dickinson and Company2023-11-272770
K213670BD Vacutainer K2EDTA Blood Collection Tubes, BD Vacutainer KBecton, Dickinson and Company2023-08-256410
K162723TransFix/EDTA Vacuum Blood Collection TubesCaltag Medsystems, Ltd.2017-06-222660
K080552CYTO-CHEX BCTStreck2008-07-311541
K012152DS30 HCY BLOOD COLLECTION TUBESDrew Scientific , Ltd.2001-09-18690
K971449VACUTAINER BRAND PLUS TUBE WITH EDTA ANTICOAGULANT(MULTIPLE)Becton Dickinson Vacutainer Systems1997-06-17571
K971221GREINER VACUETTE BLOOD COLLECTION TUBEGreiner America, Inc.1997-05-02305
K951886LOK-ON NEEDLE DISPOSAL SYSTEMBecton Dickinson Vacutainer Systems1995-06-30670
K945458VACUTAINER BRAND SAFETY-GARD PHLEBOTOMY SYSTEMBd Becton Dickinson Vacutainer Systems Preanalytic1995-02-06910
K944814CORVAC PLASTIC BLOOD COLLECTION TUBESherwood Medical Co.1994-12-19810
K940058MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPERSherwood Medical Co.1994-05-021170
K933939BACT/ALERT BLOOD COLLECTION ADAPTER CAP AND INSERTOrganon Teknika Corp.1994-02-071791
K933386VACUTAINER BRAND SAFETY-GARD NEEDLE HOLDER & NEEDLE DISPOSABBd Becton Dickinson Vacutainer Systems Preanalytic1993-10-12920
K922858MULTIDRAW SYSTEMCambridge Multi-Draw, Inc.1992-11-161540
K922468ANGEL WING SETS -- MODIFIEDMbo Laboratories, Inc.1992-07-10580
K921778DIRECTDRAW SUPERSERUMInternational Technidyne Corp.1992-05-28440
K921636VACUTAINER(R) BRAND SAFETY-LOK BLOOD COLLECT SETBd Becton Dickinson Vacutainer Systems Preanalytic1992-04-29230
K920184ANGEL WING SAFETY BLOOD COLLECTION WITH TUBE HOLD.Mbo Laboratories, Inc.1992-02-18340
K914901VACUTAINER KITAbbott Laboratories1992-01-08680
K915213CORVAC BLOOD COLLECTION TUBESherwood Medical Co.1992-01-08510
K8963731400 SERIES EVIDENCE COLLECTION KITTransidyne General Corp.1990-02-261120
K896514QS90 SMOOTH E ARTERIAL BLOOD SAMPLERRadiometer America, Inc.1990-01-23700
K882501ACCUFIBRIN(TM) BLOOD COLLECTION SYSTEM AF100Terumo Medical Corp.1988-07-18310
K861449VACUUM BLOOD COLLECTING SYSTEM (NEO-TUBE)Exel Intl.1986-09-161520
K803182SYRINGE FOR BLOOD SAMPLINGThe University of Chicago1981-01-16310
K801015PREZAPAK L ARTERIAL BLOOD SAMPLING KITKimble-Terumo, Inc.1980-05-14150
K791200PRE-DENTFichte, Graves, and Hunt1979-08-10430
K771874J-VAC VACUUM TUBEJelco Laboratories1977-12-02600
K771985FILTER SAMPLER BLOOD SERUM FILTERClasrock1977-11-02140
K771305LIQUAEMIN SODIUM, HEPARIN SODIUM ETC.Organon, Inc.1977-08-04210
K771304LIQUAEMIB SODIUM PRESERVATIVE, ETC.Organon, Inc.1977-08-04210
K771053BLOOD COLLECTION TUBE, GRAYSherwood Medical Industries1977-06-29160
K771055BLOOD COLLECTION TUBE, REDSherwood Medical Industries1977-06-29160
K771056BLOOD COLLECTION TUBE, GREENSherwood Medical Industries1977-06-29160
K771054BLOOD COLLECTION TUBE, BLUESherwood Medical Industries1977-06-29160
K771052BLOOD COLLECTION TUBE, LAVENDERSherwood Medical Industries1977-06-27140
K760019VACUUM TUBES, PEDIATRIC SIZES (J-VAC)Jelco Laboratories1976-07-20390
K760018VACUUM TUBES, STERILE (J-VAC)Jelco Laboratories1976-07-20390

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