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U.S. Department of Health and Human Services

510(k) Premarket Notification
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51 to 60 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
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arthrocare controller, arthrocare cable, footswitch, powercord ARTHROCARE CORP. K001936 07/19/2000
arthrocare flow control unit ARTHROCARE CORP. K001904 07/17/2000
arthrocare system 2000 controller, arthrocare system 2000 cable, arthrocare system 2000 footswitch, plasma scalpel gs, c ARTHROCARE CORP. K001302 05/30/2000
entec reflex wand 55, model e4055-01, e4045-01 ARTHROCARE CORP. K000778 05/03/2000
visage cosmetic surgery, model v5000 ARTHROCARE CORP. K992180 03/20/2000
modification to arthrocare controller, arthrocare cable, footswitch, powercord, arthrowands and spine wands ARTHROCARE CORP. K000511 03/13/2000
entec controller, entec patient cable, footswitch, powercord, plasma wand ARTHROCARE CORP. K000228 02/22/2000
arthrocare controller, arthrocare cable, footswitch, powercord, plasma scalpel gs, turbovac gs ARTHROCARE CORP. K000074 02/04/2000
entec reflex wand 55, model e4055-00 ARTHROCARE CORP. K000036 02/04/2000
arthrocare controller, arthrocare cable, footswitch, powercord, arthrowands and spinewands ARTHROCARE CORP. K000044 02/01/2000
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