IN VITRO DIAG. FOR URIC ACID— 510(k) K770767

Substantially Equivalent

Smithkline Diagnostics, Inc.

FDA 510(k) clearance K770767 for IN VITRO DIAG. FOR URIC ACID, Substantially Equivalent on 1977-07-05. Applicant: Smithkline Diagnostics, Inc..

Clearance details

Applicant: Smithkline Diagnostics, Inc.
Product code: Code CDO
Advisory panel: Clinical Chemistry
Date received: 1977-04-28
Decision date: 1977-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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