LIGHT DIAGNOSTICS RABIES DFA REAGENT— 510(k) K972975

Name: FDA 510(k) clearance K972975
Creator: U.S. Food and Drug Administration
Published: 1998-12-22

Substantially Equivalent

Light Diagnostics

FDA 510(k) clearance K972975 for LIGHT DIAGNOSTICS RABIES DFA REAGENT, Substantially Equivalent on 1998-12-22. Applicant: Light Diagnostics. Device class: 2.

Clearance details

Applicant: Light Diagnostics
Product code: Code GOI
Device class: Class 2
Regulation: 21 CFR 866.3460
Advisory panel: Microbiology
Date received: 1997-08-11
Decision date: 1998-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Temecula, CA, US

Download summary PDF View on FDA.gov ↗

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