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FDA 510(k), K172819, LightWalker Laser System Family
FDA 510(k), K172819, LightWalker Laser System Family
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510(K) Number: K172819
Device Name: LightWalker Laser System Family
Manufacturer: Marko Berdajs
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: KXA
Date Received: 09/18/2017
Decision Date: 12/01/2017
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LightWalker Laser System Family
Manufacturer: Marko Berdajs
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: KXA
Date Received: 09/18/2017
Decision Date: 12/01/2017
Decision: Substantially Equivalent (SESE)
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
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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