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FDA 510(k) Applications for Medical Device Product Code "ORQ"
FDA 510(k) Number
Applicant
Device Name
Decision Date
K121139
Covidien LLC
ACCUMESH DEPLOYMENT SYSTEM
05/02/2012
K123066
Covidien LLC
ACCUMESH DEPLOYMENT SYSTEM
10/16/2012
K130782
Covidien LLC
ACCUMESH DEPLOYMENT SYSTEM
04/05/2013
K101218
POLYTOUCH MEDICAL LTD
PATCHASSIST
06/17/2010
K103269
POLYTOUCH MEDICAL LTD
PATCHASSIST LARGE
11/23/2010
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