Reprocessed DePuy Mitek Ablation Wand— 510(k) K173740
Substantially EquivalentRenovo, Inc.
FDA 510(k) clearance K173740 for Reprocessed DePuy Mitek Ablation Wand, Substantially Equivalent on 2018-03-19. 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
Recent devices under product code NUJ
view all- K232511 — Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)
- K230251 — Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
- K220411 — Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
- K211203 — Green OR Reprocessed Aquamantys Bipolar Sealer
- K191073 — Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter
More clearances from Renovo, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.