MODIFICATION TO PLUM XL INFUSION PUMP


Device Classification Name

pump, infusion

510(k) Number K010924
Device Name MODIFICATION TO PLUM XL INFUSION PUMP
Original Applicant
ABBOTT LABORATORIES
dept.37k, building ap30
200 abbott park road
abbott park, 
IL 
60064 -6157

Original Contact frank pokrop
Regulation Number 880.5725
Classification Product Code
FRN  
Date Received 03/27/2001
Decision Date 04/06/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls