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FDA 510(k) Application Details - K010890
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K010890
Device Name
Syringe, Piston
Applicant
BECTON DICKINSON AND CO.
1 BECTON DR.
FRANKLIN LAKES, NJ 07417-1880 US
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Contact
PETER ZURLO
Other 510(k) Applications for this Contact
Regulation Number
880.5860
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Classification Product Code
FMF
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More FDA Info for this Product Code
Date Received
03/26/2001
Decision Date
04/19/2001
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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