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FDA 510(k), K152570, Bovie J-Plasma Precise 360 Handpiece
FDA 510(k), K152570, Bovie J-Plasma Precise 360 Handpiece
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$149.00 USD
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$149.00 USD
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510(K) Number: K152570
Device Name: Bovie J-Plasma Precise 360 Handpiece
Manufacturer: BOVIE MEDICAL CORPORATION
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 09/09/2015
Decision Date: 11/02/2015
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Bovie J-Plasma Precise 360 Handpiece
Manufacturer: BOVIE MEDICAL CORPORATION
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 09/09/2015
Decision Date: 11/02/2015
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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