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FDA 510(k) Application Details - K042934
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K042934
Device Name
Syringe, Piston
Applicant
BECTON DICKINSON & CO.
1 Becton Drive
Franklin Lakes, NJ 07417 US
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Contact
PETER ZURLO
Other 510(k) Applications for this Contact
Regulation Number
880.5860
More FDA Info for this Regulation Number
Classification Product Code
FMF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/25/2004
Decision Date
10/28/2004
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
Y
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