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FDA 510(k) Application Details - K170386
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K170386
Device Name
Syringe, Piston
Applicant
Becton, Dickinson & Company
1 Becton Drive
Franklin Lakes, NJ 07666 US
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Contact
Riddhish Patel
Other 510(k) Applications for this Contact
Regulation Number
880.5860
More FDA Info for this Regulation Number
Classification Product Code
FMF
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More FDA Info for this Product Code
Date Received
02/08/2017
Decision Date
04/12/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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