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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Powered Laser Surgical Instrument
510(k) Number K041957
Device Name EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
Applicant
Diomed, Inc.
5 Timber Lane
North Reading,  MA  01864
Applicant Contact MAUREEN O'CONNELL
Correspondent
Diomed, Inc.
5 Timber Lane
North Reading,  MA  01864
Correspondent Contact MAUREEN O'CONNELL
Regulation Number878.4810
Classification Product Code
GEX  
Date Received07/21/2004
Decision Date 12/01/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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