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

Light Diagnostics — Predicate Candidate Screening

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

498 daysmedian FDA review time
617 days90th percentile
19clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K991880LIGHT DIAGNOSTICS SIMULFLUOR HSV 1/2 IMMUNOFLUORECENCE ASSAYLight Diagnostics1999-11-091600
K990141LIGHT DIAGNOSTICS SIMULFLUOR HSV/VZV IMMUNOFLOURESCENCE ASSALight Diagnostics1999-10-192730
K972975LIGHT DIAGNOSTICS RABIES DFA REAGENTLight Diagnostics1998-12-224980
K974302LIGHT DIAGNOSTICS SIMULFLUOR FLU A/FLU BLight Diagnostics1998-04-081422
K951821CYTOMEGALOVIRUS DIRECT IMMUNOFLUORESCENCE ASSAYLight Diagnostics1996-06-074140
K951799VARICELLA-ZOSTER VIRUS DIRECT IMMUNOFLUORESCENCE ASSAYLight Diagnostics1996-03-203360
K940026POLIOVIRUS BLEND MONOCLONAL ANTIBODIESLight Diagnostics1995-09-126170
K940034POLIOVIRUS 2 MONOCLONAL ANTIBODYLight Diagnostics1995-09-126160
K940017POLIOVIRUS 3 MONOCLONAL ANTIBODYLight Diagnostics1995-09-126160
K936254COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODYLight Diagnostics1995-09-086170
K936251COXSACKIEVIRUS B3 MONOCLONAL ANTIBODYLight Diagnostics1995-09-086170
K936252COXSACKIEVIRUS B@ MONOCLONAL ANTIBODYLight Diagnostics1995-09-086170
K940018POLIOVIRUS 1 MONOCLONAL ANTIBODYLight Diagnostics1995-09-086120
K940363ENTEROVIRUS 70 MONCLONAL ANTIBODYLight Diagnostics1995-09-085900
K936253COXSACKIEVIRUS B4 MONOCLONAL ANTIBODYLight Diagnostics1995-09-086170
K944191ANTI-NUCLEAR ANTIBODY(ANA) TEST KIT W/MOUSE LIVERLight Diagnostics1995-03-061890
K944192ANTI-NUCLEAR ANTIBODY (ANA) TEST KIT W/RAT LIVERLight Diagnostics1995-03-061890
K935809CYTOMEGALOVIRUS INDIRECT IMMUNOFLUORESCENCE ASSAYLight Diagnostics1994-05-051540
K922801RESP. PANEL 1 INDIRECT IMMUNOFLUORESCENCE ASSAYLight Diagnostics1993-01-062100

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