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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
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arthrocare controller (system 12000), arthrocare patient cable, foot control, power cord, wands ARTHROCARE CORP. K082666 10/15/2008
arthrocare controller (system 2000 and 8000), arthrocare patient cable, foot control, power cord and wands ARTHROCARE CORP. K063538 12/01/2006
arthrocare controller (system 2000 and 8000); arthrocare cable; foot control; power cord; and wands ARTHROCARE CORP. K020622 03/28/2002
arthrocare controller (system 2000 and 8000); arthrocare patient cable; foot control; power cord; wands ARTHROCARE CORP. K030551 03/07/2003
arthrocare controller, arthrocare cable, foot control, power cord, wands ARTHROCARE CORP. K020832 04/09/2002
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
arthrocare controller, arthrocare cable, footswitch, powercord, plasma scalpel gs, turbovac gs ARTHROCARE CORP. K000074 02/04/2000
arthrocare controller, arthrocare cable, footswitch, powercord, spine wands, orthowands, arthrowands ARTHROCARE CORP. K992581 12/09/1999
arthrocare controller, authrocare cable, foot control, power cord, wands ARTHROCARE CORP. K021519 06/06/2002
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