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FDA 510(k) Application Details - K170722
Device Classification Name
Pump, Breast, Powered
More FDA Info for this Device
510(K) Number
K170722
Device Name
Pump, Breast, Powered
Applicant
Moxxly, Inc.
1777 Yosemite Ave. Suite 235
San Francisco, CA 94124 US
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Contact
Cara Delzer
Other 510(k) Applications for this Contact
Regulation Number
884.5160
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Classification Product Code
HGX
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More FDA Info for this Product Code
Date Received
03/09/2017
Decision Date
08/28/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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