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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name pump, breast, powered
510(k) Number K021739
Device Name LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002
Applicant
LIMERICK, INC.
903 NORTH SAN FERNANDO BLVD.
SUITE 5
BURBANK,  CA  91504
Applicant Contact PATRICIA KELLY
Correspondent
LIMERICK, INC.
903 NORTH SAN FERNANDO BLVD.
SUITE 5
BURBANK,  CA  91504
Correspondent Contact PATRICIA KELLY
Regulation Number884.5160
Classification Product Code
HGX  
Date Received05/28/2002
Decision Date 01/10/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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