FDA 510(k), K070374, ARTHROCARE ENT PLASMA WAND

FDA 510(k), K070374, ARTHROCARE ENT PLASMA WAND

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510(K) Number: K070374
Device Name: ARTHROCARE ENT PLASMA WAND
Manufacturer: ARTHROCARE CORP.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 02/08/2007
Decision Date: 04/25/2007
Regulation Medical Specialty: General & Plastic Surgery
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