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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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system 2000 controller, system 5000 controller, footswitch, power cord, and visage wandsff ARTHROCARE CORP. K020408 05/02/2002
arthrocare arthro wands, enetec evac plasma wand ARTHROCARE CORP. K013463 11/15/2001
arthrocare controller, model h2000; arthrocare cable, model h0970-02; footswitch, model h2000-04; powercord, model h2000 ARTHROCARE CORP. K011634 06/19/2001
arthrocare controller, patient cable, foot control, power cord ARTHROCARE CORP. K014222 01/18/2002
arthrocare electrosurgery wands ARTHROCARE CORP. K012519 10/25/2001
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
entec plasma wands ARTHROCARE CORP. K014290 03/28/2002
arthrocare controller, arthrocare cable, footswitch, powercord ARTHROCARE CORP. K001936 07/19/2000
arthrocare controller, arthrocare cable, footswitch, powercord, arthrowands and spinewands ARTHROCARE CORP. K000044 02/01/2000
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