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U.S. Department of Health and Human Services

510(k) Premarket Notification
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31 to 40 of 45 Results
ProductCode: GDW Applicant: Covidien Decision Date To: 05/21/2024
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endo gia radial reload with tri-staple technology COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K131705 07/01/2013
endo gia reload COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K130717 04/18/2013
reliamax gastrointestinal anastomosis and reload COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K122781 02/05/2013
idrive ultra powered handle and endo gia adapter COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K123318 12/18/2012
absorbatack 5mm single use absorbable fixation device COVIDIEN K123109 10/23/2012
idrive ultra powered handle endo gia adapter COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K121510 07/25/2012
duet trs reloads, duet trs reloads with tri-staple technology, endo gia universal and ultra universal staplers COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K120258 02/29/2012
endo gia(tm) staplers, dst series(tm) gia(tm) staplers, dst series(tm) ta(tm) staplers COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K111825 10/25/2011
endo gia singleuse duet trs reload with tri0staple technology COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H K103263 11/22/2010
idrive system (i drive power handle, idrive (ralc) single use reload) COVIDIEN LLC, FORMERLY REGISTERED AS TYCO HEALTHCA K102325 10/13/2010
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