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FDA 510(k), K022060, LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES
FDA 510(k), K022060, LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES
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510(K) Number: K022060
Device Name: LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES
Manufacturer: ANNE WORDEN
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: 06/25/2002
Date Received: 10/30/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES
Manufacturer: ANNE WORDEN
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: 06/25/2002
Date Received: 10/30/2002
Decision Date: Substantially Equivalent (SESE)
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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