Reprocessed Vessel Sealer— 510(k) K152134
Substantially EquivalentSterilmed, Inc.
FDA 510(k) clearance K152134 for Reprocessed Vessel Sealer, Substantially Equivalent on 2016-01-15. Applicant: Sterilmed, Inc..
Clearance details
- Applicant
- Sterilmed, Inc.
- Product code
- Code NUJ
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.