VIDAS ROTAVIRUS (RTV) ASSAY— 510(k) K972895

Name: FDA 510(k) clearance K972895
Creator: U.S. Food and Drug Administration
Published: 1997-10-03

Substantially Equivalent

Biomerieux Vitek, Inc.

FDA 510(k) clearance K972895 for VIDAS ROTAVIRUS (RTV) ASSAY, Substantially Equivalent on 1997-10-03. Applicant: Biomerieux Vitek, Inc.. Device class: 1.

Clearance details

Applicant: Biomerieux Vitek, Inc.
Product code: Code LIQ
Device class: Class 1
Regulation: 21 CFR 866.3405
Advisory panel: Microbiology
Date received: 1997-08-05
Decision date: 1997-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockland, MA, US

Download summary PDF View on FDA.gov ↗

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