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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, suction, lipoplasty for removal
510(k) Number K081593
Device Name POWER ASPIRATOR, MODEL LS2 OR LS2DP
Applicant
MEDICAL DEVICE RESOURCE CORP.
23392 CONNECTICUT ST.
HAYWARD,  CA  94545
Applicant Contact MEL KIMSEY
Correspondent
MEDICAL DEVICE RESOURCE CORP.
23392 CONNECTICUT ST.
HAYWARD,  CA  94545
Correspondent Contact MEL KIMSEY
Regulation Number878.5040
Classification Product Code
QPB  
Date Received06/06/2008
Decision Date 07/23/2008
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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