ACCUMESH DEPLOYMENT SYSTEM— 510(k) K123066

Substantially Equivalent

Covidien, LLC

FDA 510(k) clearance K123066 for ACCUMESH DEPLOYMENT SYSTEM, Substantially Equivalent on 2012-10-16. 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.