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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
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arthrocare controller, model h2000; arthrocare cable, model h0970-02; footswitch, model h2000-04; powercord, model h2000 ARTHROCARE CORP. K011634 06/19/2001
arthrocare system 2000 controller, cable, footswitch, power cord & arthrocare arthrowand ARTHROCARE CORP. K011083 06/28/2001
entec evac plasma wand ARTHROCARE CORP. K011279 07/19/2001
arthrocare electrosurgery wands ARTHROCARE CORP. K012519 10/25/2001
arthrocare arthro wands, enetec evac plasma wand ARTHROCARE CORP. K013463 11/15/2001
arthrocare controller, patient cable, foot control, power cord ARTHROCARE CORP. K014222 01/18/2002
arthrocare controller; arthrocare cable; foot control; power cord; wands ARTHROCARE CORP. K020557 03/21/2002
arthrocare controller (system 2000 and 8000); arthrocare cable; foot control; power cord; and wands ARTHROCARE CORP. K020622 03/28/2002
entec plasma wands ARTHROCARE CORP. K014290 03/28/2002
arthrocare controller, arthrocare cable, foot control, power cord, wands ARTHROCARE CORP. K020832 04/09/2002
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