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FDA 510(k) Application Details - K023752
Device Classification Name
Syringe, Piston
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510(K) Number
K023752
Device Name
Syringe, Piston
Applicant
BD
ONE BECTON DRIVE MC226
FRANKLIN LAKES, NJ 07417 US
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PASQUALE AMATO
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Regulation Number
880.5860
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Classification Product Code
FMF
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Date Received
11/08/2002
Decision Date
02/07/2003
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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