FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DK*300 VOLUMETRIC INFUSION CONTROLLER

K Number: K843254 · Decision Oct 11, 1984
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
59
Applicant Total
10
Review Days
52

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Basic Information

Device Name
DK*300 VOLUMETRIC INFUSION CONTROLLER
K Number
K843254
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Deka Research & Development Corp.
Date Received
August 20, 1984
Decision Date
October 11, 1984
Product Code
LDR
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LDR Controller, Infusion, Intravascular, Electronic

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