Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves— 510(k) K172097
Substantially EquivalentRenovo, Inc.
FDA 510(k) clearance K172097 for Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves, Substantially Equivalent on 2017-10-06. Applicant: Renovo, Inc.. Device class: 2.
Clearance details
- Applicant
- Renovo, Inc.
- Product code
- Code NLM
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- 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.