IN VITRO DIAGNOSTIC TEST— 510(k) K770467

Substantially Equivalent

Hoffmann-La Roche, Inc.

FDA 510(k) clearance K770467 for IN VITRO DIAGNOSTIC TEST, Substantially Equivalent on 1977-04-27. Applicant: Hoffmann-La Roche, Inc..

Clearance details

Applicant: Hoffmann-La Roche, Inc.
Advisory panel: Unknown
Date received: 1977-03-10
Decision date: 1977-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.