Atlas FDA

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

LRM — Predicate Candidate Screening

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

77 daysmedian FDA review time
223 days90th percentile
29clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K101319IMMULISA DSDNA ANTIBODY ELISAImmco Diagnostics, Inc.2010-12-092120
K083381EUROIMMUN ANTI-DSDNA-NCX ELISA (IGG)Euroimmun Us, Inc.2009-04-151520
K062183FARRZYME HUMAN HIGH AVIDITY ANTI-DSDNA ENZYME IMMUNOASSAY KIThe Binding Site, Ltd.2006-11-211130
K040811VARELISA SSDNA ANTIBODIES, MODEL 14896Pharmacia Deutschland GmbH2004-05-13450
K001900ENZYME IMMUNOASSAY ANTI-SSDNA ANTIBODY TESTHelix Diagnostics, Inc.2000-09-11810
K000477MDI DS-DNA TESTMicro Detect, Inc.2000-03-01160
K994424DIAMEDIX IS-ANTI-DSDNA TEST SYSTEMDiamedix Corp.2000-02-18500
K993727BINDAZYME ANTI-DSDNA EIA KITThe Binding Site, Ltd.1999-12-21570
K984396LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213Bio-Rad1998-12-1890
K983422THE APTUS (AUTOMATED) APPLICATIONS OF THE DS DNA ELISA TEST Zeus Scientific, Inc.1998-11-18500
K980391SERAQUEST ANTI-DSDNAQuest Intl., Inc.1998-04-24810
K974694IS-DSDNA TEST SYSTEMDiamedix Corp.1998-03-03770
K962730HYCOR HY.TEC/MANUAL DS-DNA AUTO-ANTIBODYHycor Biomedical, Inc.1997-03-072490
K952567AUTOSTATTMII ANTI-DSDNACogent Diagnotics , Ltd.1997-03-046380
K960182DSDNA IMMUNOGLOBULIN EIA TEST SYSTEMMardx Diagnostics, Inc.1996-03-20640
K960091ENZYME IMMUNOASSAY ANTI-DOUBLE STRANDED DNA (DSDNA) TEST KITHelix Diagnostics, Inc.1996-03-20692
K954893HYTEC AUTOMIMMUNE KIT (DS-DNA)Hycor Biomedical, Inc.1996-03-201470
K953671ORGEN TEC ANTI-DSDNA ELISA ASSAYOrgentec1995-11-09940
K952055ORGEN TEC ANTI-DSDNA PIN IMMUNO ASSAYAmerican Laboratory Products Co., Ltd.1995-07-18770
K944334VARELISA COMBINED DNA ANTIBODIES EIAElias U.S.A., Inc.1995-04-172230
K950031VARELISA DSDNA ANTIBODIES (FARR VERSION)Elias U.S.A., Inc.1995-03-10650
K940585SELISA ANTI-N DNA ANTIBODIESCambridge Life Sciences Plc.1994-06-101220
K923537ENCORE DS-DNAClark Laboratories, Inc.1992-12-231600
K9136533M ANTI-DSDNA FAST TEST3M Diagnostic Systems, Inc.1991-11-07830
K912020ANTI-DNA MICROASSAYDiamedix Corp.1991-09-231390
K902897UBI MAGIWEL(TM) ANTI-DS-DNA QUANTITATIVEUnited Biotech, Inc.1990-07-16130
K893036ANTI-DSDNA KIT, IM.77/771 (50/100 TEST KITS)Amersham Corp.1989-06-02390
K874191NDNA ANTIBODY TEST KITLipogen, Inc.1987-12-18650
K870903IMMUSTRIP(TM) DSDNA ELISA TEST SYSTEMImmunomedics, Inc.1987-05-14700

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