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FDA 510(k), K060555, SPRAYGENIX CRYO ABLATION SYSTEM
FDA 510(k), K060555, SPRAYGENIX CRYO ABLATION SYSTEM
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510(K) Number: K060555
Device Name: SPRAYGENIX CRYO ABLATION SYSTEM
Manufacturer: CRYMED TECHNOLOGIES, INC.
Device Classification Name: unit, cryosurgical, accessories
Regulation Number: 878.4350
Classification Product Code: GEH
Date Received: 03/02/2006
Decision Date: 04/21/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SPRAYGENIX CRYO ABLATION SYSTEM
Manufacturer: CRYMED TECHNOLOGIES, INC.
Device Classification Name: unit, cryosurgical, accessories
Regulation Number: 878.4350
Classification Product Code: GEH
Date Received: 03/02/2006
Decision Date: 04/21/2006
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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