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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 K151632
Device Name Symphony Breastpump, Symphony reconditioned, Symphony Preemie+ Breastpump, Symphony Plus Breastpump (battery version), Symphony Consignment, Preemie Consignment Pump, Symphony Rental, Symphony Plus Rental, Symphony Preemie+ Rental
Applicant
MEDELA AG
LATTICHSTRASSE 4B
BAAR,  CH 6341
Applicant Contact Orlando Antunes
Correspondent
PATHWAY REGULATORY CONSULTING, LLC
W324 S3649 COUNTY ROAD E
DOUSMAN,  WI  53118
Correspondent Contact ADRIENNE LENZ
Regulation Number884.5160
Classification Product Code
HGX  
Date Received06/17/2015
Decision Date 11/05/2015
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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