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FDA 510(k) Application Details - K161667
Device Classification Name
Pump, Infusion
More FDA Info for this Device
510(K) Number
K161667
Device Name
Pump, Infusion
Applicant
Q Core Medical Ltd.
29 Yad Haruzim St.
Netanya 4250529 IL
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Contact
Shimon Vaknin
Other 510(k) Applications for this Contact
Regulation Number
880.5725
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Classification Product Code
FRN
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More FDA Info for this Product Code
Date Received
06/16/2016
Decision Date
03/27/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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