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FDA 510(k) Application Details - K010924
Device Classification Name
Pump, Infusion
More FDA Info for this Device
510(K) Number
K010924
Device Name
Pump, Infusion
Applicant
ABBOTT LABORATORIES
DEPT.37K, BUILDING AP30
200 ABBOTT PARK ROAD
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
03/27/2001
Decision Date
04/06/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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