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FDA 510(k), K130689, SYMPHONY RF GENERATOR
FDA 510(k), K130689, SYMPHONY RF GENERATOR
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510(K) Number: K130689
Device Name: SYMPHONY RF GENERATOR
Manufacturer: THERMIGEN, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 03/13/2013
Decision Date: 11/15/2013
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SYMPHONY RF GENERATOR
Manufacturer: THERMIGEN, INC.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 03/13/2013
Decision Date: 11/15/2013
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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