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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 K884682
Device Name LIVING TECHNOLOGY LASER CONTACT TIPS
Applicant
Living Technology, Inc.
440 Constance Dr.
Warminster,  PA  18974
Applicant Contact ROBERT E YOCHER
Correspondent
Living Technology, Inc.
440 Constance Dr.
Warminster,  PA  18974
Correspondent Contact ROBERT E YOCHER
Regulation Number878.4810
Classification Product Code
GEX  
Date Received11/08/1988
Decision Date 01/05/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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