TEST, IN-VITRO DIAGNOSTIC— 510(k) K760089

Substantially Equivalent

Hoffmann-La Roche, Inc.

FDA 510(k) clearance K760089 for TEST, IN-VITRO DIAGNOSTIC, Substantially Equivalent on 1976-07-20. Applicant: Hoffmann-La Roche, Inc..

Clearance details

Applicant: Hoffmann-La Roche, Inc.
Advisory panel: Unknown
Date received: 1976-06-21
Decision date: 1976-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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