ACCUMESH DEPLOYMENT SYSTEM— 510(k) K121139
Substantially EquivalentCovidien, LLC
FDA 510(k) clearance K121139 for ACCUMESH DEPLOYMENT SYSTEM, Substantially Equivalent on 2012-05-02. Applicant: Covidien, LLC. Device class: 2.
Clearance details
- Applicant
- Covidien, LLC
- Product code
- Code ORQ
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Bedford, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.