VITROS IMMUNODIAGNOSTIC PRODUCTS RANGE VERIFIERS— 510(k) K973517

Substantially Equivalent

Johnson & Johnson Clinical Diagnostics, Inc.

FDA 510(k) clearance K973517 for VITROS IMMUNODIAGNOSTIC PRODUCTS RANGE VERIFIERS, Substantially Equivalent on 1997-09-25. Applicant: Johnson & Johnson Clinical Diagnostics, Inc..

Clearance details

Applicant: Johnson & Johnson Clinical Diagnostics, Inc.
Product code: Code JJY
Advisory panel: Clinical Chemistry
Date received: 1997-09-17
Decision date: 1997-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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