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FDA 510(k), K060232, TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES
FDA 510(k), K060232, TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES
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510(K) Number: K060232
Device Name: TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES
Manufacturer: TROKAMED GMBH
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 01/30/2006
Decision Date: 07/12/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES
Manufacturer: TROKAMED GMBH
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 01/30/2006
Decision Date: 07/12/2006
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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