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

LKJ — Predicate Candidate Screening

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

62 daysmedian FDA review time
228 days90th percentile
50clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K210902EliA Ro52, EliA Ro60Phadia AB2022-07-274880
K113610ANA-SCREEN WITH MDSSBio-Rad Laboratories2012-07-092160
K082759ELIA CENP IMMUNOASSAY, ELIA U1RNP IMMUNOASSAY, ELIA SM IMMUNPhadia US, Inc.2009-04-102000
K081104AESKULISA ANA HEP-2, REF 30-7115USAesku Diagnostics2008-05-02140
K041658BIOPLEX 200 ANA SCREEN ON THE BIOPLEX 2200 MULTI-ANALYTE DETBio-Rad Laboratories, Inc.2004-12-201850
K042416ATHENA MULTI-LYTE ANA-II TEST SYSTEMZeus Scientific, Inc.2004-10-08310
K034013REAADS DSDNA QUANTITATIVE TEST KIT, MODEL 022-001Corgenix, Inc.2004-01-08150
K030775AUTO I.D. JO-1, SCL-70 & PCNA POSITIVE CONTROL SERUMImmuno Concepts, N.A. , Ltd.2003-05-12620
K024218LIQUICHEK ANTI-SS-A CONTROL, POSITIVE, CATALOG #114Bio-Rad2003-01-17250
K024232LIQUICHEK ANTI-SS-B CONTROL, POSITIVE, CATALOG #113Bio-Rad2003-01-17250
K024223LIQUICHEK ANTI-RNP CONTROL, POSITIVE, CATALOG #116Bio-Rad2003-01-13210
K024226LIQUICHEK ANTI-SCL-70 CONTROL, POSITIVE, CATALOG #116Bio-Rad2003-01-10180
K021257ANA LINE BLOT, CATALOG NUMBER: KALABI (20 TESTS)Diagnostic Products Corp.2002-06-03450
K021103MODIFICATION TO ZEUS SCIENTIFIC'S ATHENA MULTI-LYTE ANA TESTZeus Scientific, Inc.2002-04-24190
K011244ZEUS SCIENTIFIC, INC. ATHENA MULTI-LYTE ANA TEST SYSTEMZeus Scientific, Inc.2001-12-102310
K993294DIAMEDIX IS-ANA ELISA SCREEN TEST SYSTEMDiamedix Corp.1999-10-25240
K984473LIQUICHEK ANA CONTROL, EIA SCREEN, MODEL 205Bio-Rad1998-12-2260
K984470LIQUICHEK ANTI-SS-A CONTROL, EIA, MODEL 209Bio-Rad1998-12-2260
K984478LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210Bio-Rad1998-12-2260
K984464LIQUICHEK ANTI-JO 1 CONTROL, EIA, MODEL NO. 211Bio-Rad1998-12-2260
K984475LIQUICHEK ANTI-SCL-70 CONTROL, EIA, MODEL 212Bio-Rad1998-12-2260
K961815QUALITROL ANA CONTROL SERUM SETConsolidated Technologies, Inc.1996-09-271400
K954392HYTEC AUTOIMMUNE KIT (SS-A)Hycor Biomedical, Inc.1995-12-26980
K954891HYTEC AUTOIMMUNE KITS (SS-B)Hycor Biomedical, Inc.1995-12-26980
K954723ENZYME IMMUNOASSAY ANA SCREENING TEST KITHelix Diagnostics, Inc.1995-12-15636
K954700ENZYME IMMUNOASSAY LUPUS SCREEN TEST KITHelix Diagnostics, Inc.1995-12-15640
K932876DIASTAT ANTI-NUCLEAR ANTIBODY (ANA) KITShield Diagnostics, Ltd.1993-11-151541
K931255SYNELISA CENP-B ANTIBODIESElias U.S.A., Inc.1993-09-241960
K932679RHEUMELISA II HISTONE ANTIBODY TEST KITBiowhittaker Molecular Applications, Inc.1993-08-23820
K932302SYLNELISA HISTONE ANTIBODIESElias U.S.A., Inc.1993-08-231030
K921132SYN ELISA DSDNA ANTIBODIESElias U.S.A., Inc.1992-12-012660
K914454THE THERATEST EL-ANA PROFILESTheratest Laboratories, Inc.1992-05-222280
K913342AUTOSTAT(TM) ANTI-DSNACogent Diagnotics , Ltd.1992-05-012800
K920150ENCORE SCL-70Clark Laboratories, Inc.1992-03-18650
K914550ANTINUCLEAR ANTIBODY IMMUNOGLOBULIN TEST SYSTEMDiagnostic Resources, Inc.1992-02-111230
K912291DISTAT ANTI-SCL-70 KITShield Diagnostics, Ltd.1991-07-30681
K894411SERATEST ENA [SCL-70] KITHemagen Diagnostics, Inc.1989-08-02160
K893896QUANTITATIVE ASSAY FOR DET. OF IGG IGM ANTI-DSDNABiostar Medical Products, Inc.1989-07-14450
K893897SEMI-QUANTITATIVE ASSAY FOR DET. OF IGG AND IGMBiostar Medical Products, Inc.1989-06-23240
K885224ANA-5 AUTOANTIBODY PROFILE KITAutoimmunity Diagnostics Corp.1989-04-141150
K883949ANTINUCLEAR ANTIBODY (ANA) TEST (MOUSE LIVER SECT)Immco Diagnostics, Inc.1988-10-27380
K883883ANTINUCLEAR ANTIBODY (ANA) TEST (HEP-2 CELLS)Immco Diagnostics, Inc.1988-10-27440
K882740ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAYLipogen, Inc.1988-09-22830
K874115NO. 1000-H FOR IMMUNOFLUOROMETRIC DETER. OF (ANA)Sigma Diagnostics, Inc.1987-11-04260
K873249ANTINUCLEAR ANTIBODY (ANA) POSITIVE CONTROLSCytotech, Inc.1987-09-22360
K864668ANA TEST KITVal Tech Diagnostics, Inc.1987-03-121000
K862313KALLESTAD SM/RNP TEST REAGENTKallestad Laboratories, Inc.1986-08-06490
K842563SERATEST DNA DETERMINATIONSeragen Diagnostics, Inc.1984-10-251150
K842484LEAP LE TEST KITCooper Biomedical, Inc.1984-07-11160
K831463ANA-CHECKDiagnostic Technology, Inc.1983-06-08330

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