PHASE II LH KIT— 510(k) K882252

Substantially Equivalent

Vitek Systems, Inc.

FDA 510(k) clearance K882252 for PHASE II LH KIT, Substantially Equivalent on 1988-08-04. Applicant: Vitek Systems, Inc..

Clearance details

Applicant: Vitek Systems, Inc.
Product code: Code CEP
Advisory panel: Clinical Chemistry
Date received: 1988-05-31
Decision date: 1988-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockland, MA, US

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