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FDA 510(k) Application Details - K960726
Device Classification Name
Pump, Breast, Powered
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510(K) Number
K960726
Device Name
Pump, Breast, Powered
Applicant
EVENFLO CO., INC.
1333 NEW HAMPSHIRE AVE., N.W.
SUITE 400
WASHINGTON, DC 20036 US
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Contact
DONALD E SEGAL
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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
02/22/1996
Decision Date
07/22/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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