Atlas FDA

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

JJS — Predicate Candidate Screening

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

35 daysmedian FDA review time
100 days90th percentile
67clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K152553CueSee HypoxicEurotrol B.V.2016-04-222270
K150226Hematocrit and Metabolite QUALICHECKRadiometer Medical Aps2015-05-131000
K130415HIGH METABOLITE QUALICHECKRadiometer Medical Aps2013-03-26350
K130236RANGE + QUALICHECK LEVEL 1, RANGE + QUALICHECK LEVEL 2, RANGRadiometer Medical Aps2013-03-15440
K033063MISSION CONTROLSDiamond Diagnostics, Inc.2003-12-12740
K022529LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL SYNTHESIS SBio-Rad2002-08-15150
K022525LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (RADIOMETER 700Bio-Rad2002-08-15150
K003242LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL), MODEL 621Bio-Rad2000-11-30440
K003239LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (800 SERIES), MBio-Rad2000-11-30440
K002865LIQUICHEK BLOOD GAS PLUS E CONTROL, MODEL 576, 577, 578Bio-Rad2000-09-25120
K002866LIQUICHEK BLOOD GAS PLUS E CONTROL LEVEL 4, MODEL 574Bio-Rad2000-09-25120
K002536LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL, MODELS 637, 63Bio-Rad2000-08-30140
K002535LIQUICHEC BLOOD GAS PLUSE CONTROL WITH GLUCOSE, MODEL 511, 5Bio-Rad2000-08-30140
K002120LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573Bio-Rad2000-08-21390
K980135QUALICHECK5+ MODELS S7730, S7740, S7750, S7760Radiometer America, Inc.1998-01-28130
K972861IL TEST CONTRIL SPECTRUM (LEVELS 1, 2 AND 3)Instrumentation Laboratory CO1997-08-19150
K961354QUALICHECK 4 METABOLITE(S3630,S3640,S3650,S3660)Radiometer America, Inc.1996-06-14670
K961355MULTICHECKRadiometer America, Inc.1996-06-14670
K961441TONOMETERED SLAINE BLOOD GAS CONTROLInstrumentarium Corp.1996-04-30150
K955340EUROTROL GAS - ISE CONTROLDirect Solutions1995-12-26360
K952637QUALICHECK 4 GLUCOSERadiometer America, Inc.1995-09-05880
K952477STAT PROFILE ULTRA BLOOD GAS CONTROLSNova Biomedical Corp.1995-07-06370
K950902ALKO TONOMETERED SALINE CONTROLAlko Diagnostic Corp.1995-03-30300
K946224CERTAIN(R) ELITE LEVEL 1, 2 AND 3Ciba Corning Diagnostics Corp.1995-01-30770
K945860SPECTRUM CO-OXIMETER LINEARITY CONTROLPhoenix Diagnostics, Inc.1995-01-17470
K935515MULTICHECK(TM)Radiometer America, Inc.1994-04-261620
K923342MICROBACT SOLID PLATE SYSTEMSRadiometer America, Inc.1992-09-22980
K920285BLOOD GAS/ISE LINEARITY CONTROLPhoenix Diagnostics, Inc.1992-07-141740
K922357RNA MEDICAL'S EQUIL 55Bionostics, Inc.1992-06-30420
K915399QUALICHECK 4Radiometer America, Inc.1992-01-02340
K904733QUALICHECK 3Radiometer America, Inc.1990-11-02160
K901985BLOOD GAS CONTROLSPhoenix Diagnostics, Inc.1990-06-06350
K901976BLOOD GAS/CO-OXIMETRY CONTROLPhoenix Diagnostics, Inc.1990-05-31290
K901986CO-OXIMETER CONTROLSPhoenix Diagnostics, Inc.1990-05-31290
K894110QUALICHECK 2Radiometer America, Inc.1989-08-03520
K874408MULTI-FUNCTION BLOOD GAS CONTROLBionostics, Inc.1987-12-14470
K872196AQUEOUS BLOOD GAS/ELECTROLYTE CONTR LEV I,II & IIIAmerican Dade1987-07-31530
K870036BAYER HEALTHCARE RAPIDQC PLUSCiba Corning Diagnostics Corp.1987-01-1490
K855024MARQUEST QC-IV TONOMETERMarquest Medical Products, Inc.1986-04-071110
K851911MULTI FUNCTION BLOOD GAS CONTROLBionostics, Inc.1985-05-20190
K841783BLOOD GAS CONTROL, LEVEL I(ACIDOSISBionostics, Inc.1984-06-14450
K833146AQUEOUS BLOOD GAS CONTROLBionostics, Inc.1983-11-28740
K832003AQUEOUS BLOOD GAS CONTROL LEVEL I,II &American Dade1983-08-10490
K832028CERTAIN HB CO-OXIMETER CONTROLCorning Medical & Scientific1983-07-18250
K830181REFEREE BLOOD GAS ANALYZER CONTROLSAnalytical Products, Inc.1983-02-28410
K820873CORNING CERTAIN TMCorning Medical & Scientific1982-04-16180
K820705GAS-TRAK 2 SYNTHETIC BLOOD GAS CONTROLUnited Diagnostics, Inc.1982-04-01160
K820319FETAL-TEK CONTROL MATUREHelena Laboratories1982-03-25480
K820103PATHWAY PH BLOOD GAS CONTROLBeckman Instruments, Inc.1982-01-28130
K812601SQC BUFFERTransidyne General Corp.1981-10-02180

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