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FDA 510(k) Application Details - K023062
Device Classification Name
Pump, Infusion
More FDA Info for this Device
510(K) Number
K023062
Device Name
Pump, Infusion
Applicant
ABBOTT LABORATORIES INC
200 ABBOTT PARK RD.
DEPT 0389 BLDG J-45
ABBOTT PARK, IL 60064-6133 US
Other 510(k) Applications for this Company
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
09/16/2002
Decision Date
09/30/2002
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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