FISHER DIAGNOSTIC LATEST ASO TEST KIT— 510(k) K852701

Name: FDA 510(k) clearance K852701
Creator: U.S. Food and Drug Administration
Published: 1985-07-19

Substantially Equivalent

Allied Fisher Scientific

FDA 510(k) clearance K852701 for FISHER DIAGNOSTIC LATEST ASO TEST KIT, Substantially Equivalent on 1985-07-19. Applicant: Allied Fisher Scientific. Device class: 1.

Clearance details

Applicant: Allied Fisher Scientific
Product code: Code GTQ
Device class: Class 1
Regulation: 21 CFR 866.3720
Advisory panel: Microbiology
Date received: 1985-06-26
Decision date: 1985-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

Download summary PDF View on FDA.gov ↗

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