TBG DIAGNOSTIC KIT— 510(k) K820252

Substantially Equivalent

Diagnostic Reagents, Inc.

FDA 510(k) clearance K820252 for TBG DIAGNOSTIC KIT, Substantially Equivalent on 1982-05-05. Applicant: Diagnostic Reagents, Inc..

Clearance details

Applicant: Diagnostic Reagents, Inc.
Product code: Code CEE
Advisory panel: Clinical Chemistry
Date received: 1982-01-29
Decision date: 1982-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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