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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 K014035
Device Name COOLTOUCH AND COOLTOUCH-II ND:YAG LASER SYSTEMS
Applicant
Cooltouch Corp.
9085 Foothills Blvd.
Roseville,  CA  95747
Applicant Contact DONALD V JOHNSON
Correspondent
Cooltouch Corp.
9085 Foothills Blvd.
Roseville,  CA  95747
Correspondent Contact DONALD V JOHNSON
Regulation Number878.4810
Classification Product Code
GEX  
Date Received12/07/2001
Decision Date 03/07/2002
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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