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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 K950750
Device Name MEDELAS BREAST PUMP
Applicant
MEDELA, INC.
4610 PRIME PKWY.
P.O. BOX 660
MCHENRY,  IL  60050 -7005
Applicant Contact STEPHEN D SMITH
Correspondent
MEDELA, INC.
4610 PRIME PKWY.
P.O. BOX 660
MCHENRY,  IL  60050 -7005
Correspondent Contact STEPHEN D SMITH
Regulation Number884.5160
Classification Product Code
HGX  
Date Received02/17/1995
Decision Date 10/16/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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