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U.S. Department of Health and Human Services

510(k) Premarket Notification
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41 to 50 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
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arthrocare system 12000 ARTHROCARE CORP. K071709 08/07/2007
arthrocare system 15000 contoller, model 72202149, arthrocare arthrowands, model 72202139,72202141, 72202143, 72202144 ARTHROCARE CORP. K090393 06/23/2009
arthrocare system 15000 controller, arthrowands ARTHROCARE CORP. K093165 12/04/2009
arthrocare system 2000 controller, arthrocare cable, footswitch, powercord, arthrocare electrosurgery wand, models h2000 ARTHROCARE CORP. K992972 09/24/1999
arthrocare system 2000 controller, arthrocare system 2000 cable, arthrocare system 2000 footswitch, arthrocare system 20 ARTHROCARE CORP. K001588 08/17/2000
arthrocare system 2000 controller, arthrocare system 2000 cable, arthrocare system 2000 footswitch, plasma scalpel gs, c ARTHROCARE CORP. K001302 05/30/2000
arthrocare system 2000 controller, cable, footswitch, power cord & arthrocare arthrowand ARTHROCARE CORP. K011083 06/28/2001
arthrocare wands ARTHROCARE CORP. K060823 04/10/2006
athrocare topaz arthrowands ARTHROCARE CORP. K053567 03/06/2006
entec controller, entec patient cable, footswitch, powercord, plasma wand ARTHROCARE CORP. K000228 02/22/2000
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