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FDA 510(k), K151649, Valleylab FT10 Electrosurgical Platform
FDA 510(k), K151649, Valleylab FT10 Electrosurgical Platform
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510(K) Number: K151649
Device Name: Valleylab FT10 Electrosurgical Platform
Manufacturer: COVIDIEN
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 06/18/2015
Decision Date: 09/10/2015
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Valleylab FT10 Electrosurgical Platform
Manufacturer: COVIDIEN
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 06/18/2015
Decision Date: 09/10/2015
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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