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FDA 510(k), K170810, CRYOFOS
FDA 510(k), K170810, CRYOFOS
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510(K) Number: K170810
Device Name: CRYOFOS
Manufacturer: CRYOFOS Medical Gmbh
Device Classification Name: unit, cryosurgical, accessories
Regulation Number: 878.4350
Classification Product Code: GEH
Date Received: 03/17/2017
Decision Date: 09/27/2017
Regulation Medical Specialty: General & Plastic Surgery
Device Name: CRYOFOS
Manufacturer: CRYOFOS Medical Gmbh
Device Classification Name: unit, cryosurgical, accessories
Regulation Number: 878.4350
Classification Product Code: GEH
Date Received: 03/17/2017
Decision Date: 09/27/2017
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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