Reprocessed ArthroCare ENT Coblator— 510(k) K172647
Substantially EquivalentRenovo, Inc.
FDA 510(k) clearance K172647 for Reprocessed ArthroCare ENT Coblator, Substantially Equivalent on 2018-02-21. Applicant: Renovo, Inc.. Device class: 2.
Clearance details
- Applicant
- Renovo, Inc.
- Product code
- Code NUJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bend, OR, US
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More clearances from Renovo, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.