STETHOS— 510(k) K963621

Substantially Equivalent

Theratechnologies, Inc.

FDA 510(k) clearance K963621 for STETHOS, Substantially Equivalent on 1996-12-04. Applicant: Theratechnologies, Inc..

Clearance details

Applicant: Theratechnologies, Inc.
Product code: Code DQD
Advisory panel: Cardiovascular
Date received: 1996-09-06
Decision date: 1996-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Quebec, CA

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