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FDA 510(k), K033257, ARTHROCARE ENT PLASMA WANDS
FDA 510(k), K033257, ARTHROCARE ENT PLASMA WANDS
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510(K) Number: K033257
Device Name: ARTHROCARE ENT PLASMA WANDS
Manufacturer: VALERIE DEFIESTA-NG
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 10/09/2003
Date Received: 10/30/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ARTHROCARE ENT PLASMA WANDS
Manufacturer: VALERIE DEFIESTA-NG
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 10/09/2003
Date Received: 10/30/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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