information about
Device Classification Name |
electrosurgical, cutting & coagulation & accessories |
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510(k) Number | K001302 | |||
Device Name | ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, PLASMA SCALPEL GS, C | |||
Original Applicant |
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Original Contact | bruce prothro | |||
Regulation Number | 878.4400 | |||
Classification Product Code |
|
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Date Received | 04/24/2000 | |||
Decision Date | 05/30/2000 | |||
Decision |
substantially equivalent (SESE) |
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Regulation Medical Specialty |
General & Plastic Surgery |
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510k Review Panel |
General & Plastic Surgery |
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Type | Traditional | |||
Reviewed by Third Party | No | |||
Combination Product |
No |