STETHOS— 510(k) K963621
Substantially EquivalentTheratechnologies, Inc.
FDA 510(k) clearance K963621 for STETHOS, Substantially Equivalent on 1996-12-04. Applicant: Theratechnologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Theratechnologies, Inc.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Montreal, Quebec, CA
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