510(k) K011868

Device
ENTERAL EXPRES PUMP UNIT, ENTERAL EXPRES GIVING SETS
Applicant
Debio Tech SA
510(k) number
K011868
Product code
LZH
Decision
Substantially Equivalent (SESE)
Decision date
2001-09-04
Date received
2001-06-14
Regulation
880.5725
Classification name
Pump, Infusion, Enteral
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
SEAN CURRY
Address
16787 Bernardo Center Dr., Suite A-1 San Diego CA US 92128 92128

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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