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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 K023624
Device Name SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921
Applicant
Surgical Laser Technologies, Inc.
147 Keystone Dr.
Montgomeryville,  PA  18936
Applicant Contact DAVIS WOODWARD
Correspondent
Surgical Laser Technologies, Inc.
147 Keystone Dr.
Montgomeryville,  PA  18936
Correspondent Contact DAVIS WOODWARD
Regulation Number878.4810
Classification Product Code
GEX  
Date Received10/29/2002
Decision Date 01/27/2003
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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