GENERAL DIAGNOSTICS PLATELET ANTIBODY— 510(k) K841465

Name: FDA 510(k) clearance K841465
Creator: U.S. Food and Drug Administration
Published: 1984-07-02

Substantially Equivalent

General Diagnostics

FDA 510(k) clearance K841465 for GENERAL DIAGNOSTICS PLATELET ANTIBODY, Substantially Equivalent on 1984-07-02. Applicant: General Diagnostics. Device class: 2.

Clearance details

Applicant: General Diagnostics
Product code: Code LLG
Device class: Class 2
Regulation: 21 CFR 864.5425
Advisory panel: Hematology
Date received: 1984-04-09
Decision date: 1984-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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