MICROBIO. PROD. FLUORESCENT ANTIBODY— 510(k) K770801

Name: FDA 510(k) clearance K770801
Creator: U.S. Food and Drug Administration
Published: 1977-05-25

Substantially Equivalent

Pfizer Pharmaceuticals

FDA 510(k) clearance K770801 for MICROBIO. PROD. FLUORESCENT ANTIBODY, Substantially Equivalent on 1977-05-25. Applicant: Pfizer Pharmaceuticals. Device class: 1.

Clearance details

Applicant: Pfizer Pharmaceuticals
Product code: Code GMY
Device class: Class 1
Regulation: 21 CFR 866.3255
Advisory panel: Microbiology
Date received: 1977-05-02
Decision date: 1977-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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