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FDA 510(k) Application Details - K024084
Device Classification Name
Pump, Infusion
More FDA Info for this Device
510(K) Number
K024084
Device Name
Pump, Infusion
Applicant
ABBOTT LABORATORIES
200 ABBOTT PARK RD.
ABBOTT PARK, IL 60064-6157 US
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Contact
FRANK POKROP
Other 510(k) Applications for this Contact
Regulation Number
880.5725
More FDA Info for this Regulation Number
Classification Product Code
FRN
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/11/2002
Decision Date
12/31/2002
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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