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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 K993671
Device Name CANDELA SCLERO LONG PULSE DYE LASER
Applicant
Candela Corp.
530 Boston Post Rd.
Wayland,  MA  01778
Applicant Contact JOAN CLIFFORD
Correspondent
Candela Corp.
530 Boston Post Rd.
Wayland,  MA  01778
Correspondent Contact JOAN CLIFFORD
Regulation Number878.4810
Classification Product Code
GEX  
Date Received11/01/1999
Decision Date 01/24/2000
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
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