Reprocessed Covidien LigaSure 5mm, Blunt Tip, Laparoscopic Sealer/Divider— 510(k) K143260
Substantially EquivalentSterilmed, Inc.
FDA 510(k) clearance K143260 for Reprocessed Covidien LigaSure 5mm, Blunt Tip, Laparoscopic Sealer/Divider, Substantially Equivalent on 2015-02-23. Applicant: Sterilmed, Inc.. Device class: 2.
Clearance details
- Applicant
- Sterilmed, 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
- Maple Grove, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.