FDA.report

510(k) K893487

Device
Lifecare 75 Controller
Applicant
ABBOTT LABORATORIES
510(k) number
K893487
Product code
LDR
Decision
Substantially Equivalent (SESE)
Decision date
1989-07-28
Date received
1989-05-04
Regulation
880.5725
Classification name
Controller, Infusion, Intravascular, Electronic
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Related Records

Applicant Contact

Contact
FREDERICK GUSTAFSON
Address
One Abbott Park Rd. Abbott Park IL US 60064 60064

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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