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FDA 510(k), K082051, COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4
FDA 510(k), K082051, COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4
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510(K) Number: K082051
Device Name: COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4
Manufacturer: COSMAN MEDICAL, INC.
Device Classification Name: generator, lesion, radiofrequency
Regulation Number: 882.4400
Classification Product Code: GXD
Date Received: 07/18/2008
Decision Date: 10/16/2008
Regulation Medical Specialty: Neurology
Device Name: COSMAN G4 RADIOFREQUENCY GENERATOR, MODEL RFG-4
Manufacturer: COSMAN MEDICAL, INC.
Device Classification Name: generator, lesion, radiofrequency
Regulation Number: 882.4400
Classification Product Code: GXD
Date Received: 07/18/2008
Decision Date: 10/16/2008
Regulation Medical Specialty: Neurology
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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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