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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 K172376
Device Name Discovery Pico, Discovery Pico Plus
Applicant
Quanta System Spa
Via Acquedotto, 109
Samarate,  IT 20826
Applicant Contact Francesco Dell'Antonio
Correspondent
Quanta System Spa
Via Acquedotto, 109
Samarate,  IT 20826
Correspondent Contact Francesco Dell'Antonio
Regulation Number878.4810
Classification Product Code
GEX  
Date Received08/07/2017
Decision Date 10/19/2017
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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