Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

LKO — Predicate Candidate Screening

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

62 daysmedian FDA review time
232 days90th percentile
23clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K191085Maverick RNP Assay and Maverick Diagnostic SystemGenalyte, Inc.2019-10-251840
K140224EUROIMMUN EUROLINE ENA PROFILE 9AG (IGG)Euroimmun US2014-12-093140
K123261EUROIMMUN ANTI-NRNP/SM ELISA (IGG)Euroimmun US2013-06-122370
K083117ELIA RNP70 IMMUNOASSAY, ELIA SCI-70 IMMUNOASSAY AND ELIA JO-Phadia US, Inc.2009-05-282180
K071210MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006Biomedical Diagnostics (Bmd) SA2007-12-192320
K022017RHIGENE MESACUP-2 TEST RNP, MODEL M7741Rhigene, Inc.2002-08-14550
K000752RHIGENE MESACUP2 TEST- RNPRhigene, Inc.2000-05-09620
K993589VARELISA RNP ANTIBODIESPharmacia & Upjohn Co.1999-11-26350
K990624AUTOSTAT II ANTI-SM/RNP ELISACogent Diagnotics , Ltd.1999-04-28620
K984476LIQUICHEK ANTI-RNP CONTROL, EIA, MODEL 207Bio-Rad1998-12-2260
K983465THE APTUS (AUTOMATED) APPLICATION OF THE SM/RNP ELISA TEST SZeus Scientific, Inc.1998-11-18480
K954831ORGENTEC ANTI-RNP/SM PIN IMMUNO ASSAYOrgentec1996-05-082010
K954897HYTEC AUTOIMMUNE KITS (RNP)Hycor Biomedical, Inc.1996-03-221850
K940588ENZYME IMMUNOASSAY ANTI-SM/RNP ANTIBODY TEST KITHelix Diagnostics, Inc.1994-04-20710
K930142SYNELISA U1-SNRNP (68KDA)-ANTIBODIESElias U.S.A., Inc.1993-05-111190
K911849IMMUNOWELL SJOGRENS SYNDROME A (RO)ANTIBODY TESTGeneral Biometrics, Inc.1991-05-07110
K911850IMMUNWELL SJOGREN`S SYNDROME B (LA) ANTIBODY TESTGeneral Biometrics, Inc.1991-05-07110
K905193DIASTAT ANTI-LA (SS-B)Shield Diagnostics, Ltd.1990-12-13240
K905194DIASTAT ANTI-RO (SS-A)Shield Diagnostics, Ltd.1990-12-13241
K895997RHEUMELISA ASSAY FOR RNP AUTOANTIBODIESLipogen, Inc.1989-11-06240
K895338ANTI-RNP AND ANTI-SM ANTIBODY TESTImmco Diagnostics, Inc.1989-10-17470
K874152RNP ANTIBODY TEST KITLipogen, Inc.1988-03-111500
K831292ANTI-ENA TESTMeloy Laboratories, Inc.1983-07-18890

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