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FDA 510(k), K041957, EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
FDA 510(k), K041957, EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
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510(K) Number: K041957
Device Name: EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
Manufacturer: DIOMED, INC.
Device Classification Name: powered laser surgical instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 07/21/2004
Decision Date: 12/01/2004
Regulation Medical Specialty: General & Plastic Surgery
Device Name: EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
Manufacturer: DIOMED, INC.
Device Classification Name: powered laser surgical instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 07/21/2004
Decision Date: 12/01/2004
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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