U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL— 510(k) K870737

Substantially Equivalent

U. S. Diagnostics, Inc.

FDA 510(k) clearance K870737 for U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL, Substantially Equivalent on 1987-04-13. Applicant: U. S. Diagnostics, Inc..

Clearance details

Applicant: U. S. Diagnostics, Inc.
Product code: Code JJT
Advisory panel: Clinical Chemistry
Date received: 1987-02-25
Decision date: 1987-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Luis Obispo, CA, US

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