FIAX TEST KIT FOR MUMPS-G ANTIBODIES— 510(k) K872733

Name: FDA 510(k) clearance K872733
Creator: U.S. Food and Drug Administration
Published: 1987-10-06

Substantially Equivalent

Whittaker Bioproducts, Inc.

FDA 510(k) clearance K872733 for FIAX TEST KIT FOR MUMPS-G ANTIBODIES, Substantially Equivalent on 1987-10-06. Applicant: Whittaker Bioproducts, Inc.. Device class: 1.

Clearance details

Applicant: Whittaker Bioproducts, Inc.
Product code: Code GRB
Device class: Class 1
Regulation: 21 CFR 866.3380
Advisory panel: Microbiology
Date received: 1987-07-09
Decision date: 1987-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walkersville, MD, US

Download summary PDF View on FDA.gov ↗

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