IN-VITRO TEST DETERMINATION OF URIC ACID— 510(k) K854185

Substantially Equivalent

Clinical Data, Inc.

FDA 510(k) clearance K854185 for IN-VITRO TEST DETERMINATION OF URIC ACID, Substantially Equivalent on 1985-11-25. Applicant: Clinical Data, Inc..

Clearance details

Applicant: Clinical Data, Inc.
Product code: Code KNK
Advisory panel: Clinical Chemistry
Date received: 1985-10-15
Decision date: 1985-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

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