TBG DIAGNOSTIC KIT— 510(k) K811725

Substantially Equivalent

Immuno Assay Corp.

FDA 510(k) clearance K811725 for TBG DIAGNOSTIC KIT, Substantially Equivalent on 1981-07-10. Applicant: Immuno Assay Corp..

Clearance details

Applicant: Immuno Assay Corp.
Product code: Code CEF
Advisory panel: Clinical Chemistry
Date received: 1981-06-18
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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