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FDA 510(k) Application Details - K022495
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K022495
Device Name
Syringe, Piston
Applicant
GETTIG PHARMACEUTICAL INSTRUMENT CO.
ONE STREAMSIDE PL. WEST
SPRING MILLS, PA 16875-0085 US
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Contact
JAMES A BENZ
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
07/29/2002
Decision Date
10/08/2002
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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