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FDA 510(k), K102329, NANOKNIFE SYSTEM
FDA 510(k), K102329, NANOKNIFE SYSTEM
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510(K) Number: K102329
Device Name: NANOKNIFE SYSTEM
Manufacturer: ANGIODYNAMICS, INC.
Device Classification Name: low energy direct current thermal ablation system
Regulation Number: 878.4400
Classification Product Code: OAB
Date Received: 08/17/2010
Decision Date: 10/24/2011
Regulation Medical Specialty: General & Plastic Surgery
Device Name: NANOKNIFE SYSTEM
Manufacturer: ANGIODYNAMICS, INC.
Device Classification Name: low energy direct current thermal ablation system
Regulation Number: 878.4400
Classification Product Code: OAB
Date Received: 08/17/2010
Decision Date: 10/24/2011
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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