ELISA TUBE LH TEST KIT— 510(k) K920920

Substantially Equivalent

Bio Clinic Co.

FDA 510(k) clearance K920920 for ELISA TUBE LH TEST KIT, Substantially Equivalent on 1992-04-08. Applicant: Bio Clinic Co..

Clearance details

Applicant: Bio Clinic Co.
Product code: Code CEP
Advisory panel: Clinical Chemistry
Date received: 1992-02-28
Decision date: 1992-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MI, US

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