AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS— 510(k) K923133

Name: FDA 510(k) clearance K923133
Creator: U.S. Food and Drug Administration
Published: 1992-09-25

Substantially Equivalent

Microprobe Corp.

FDA 510(k) clearance K923133 for AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS, Substantially Equivalent on 1992-09-25. Applicant: Microprobe Corp.. Device class: 1.

Clearance details

Applicant: Microprobe Corp.
Product code: Code MJM
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1992-06-29
Decision date: 1992-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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