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FDA 510(k), K220426, Fiber Dust PRO
FDA 510(k), K220426, Fiber Dust PRO
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$149.00 USD
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$149.00 USD
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510(K) Number: K220426
Device Name: Fiber Dust PRO
Manufacturer: Quanta System Spa
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 02/14/2022
Decision Date: 03/16/2022
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Fiber Dust PRO
Manufacturer: Quanta System Spa
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 02/14/2022
Decision Date: 03/16/2022
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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