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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Light, Ultraviolet, Dermatological
510(k) Number K033946
Device Name LOVELY SYSTEM
Applicant
MSQ (M2) LTD.
3637 BERNAL AVENUE
PLEASANTON,  CA  94566
Applicant Contact ANNE WORDEN
Correspondent
MSQ (M2) LTD.
3637 BERNAL AVENUE
PLEASANTON,  CA  94566
Correspondent Contact ANNE WORDEN
Regulation Number878.4630
Classification Product Code
FTC  
Subsequent Product Code
GEX  
Date Received12/19/2003
Decision Date 04/05/2004
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
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