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

INTRAVENOUS INFUSION CONTROLLER

K Number: K834106 · Decision May 30, 1984
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
59
Applicant Total
39
Review Days
183

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Basic Information

Device Name
INTRAVENOUS INFUSION CONTROLLER
K Number
K834106
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Cutter Laboratories, Inc.
Date Received
November 29, 1983
Decision Date
May 30, 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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Other Clearances by Cutter Laboratories, Inc.

K Number Device Name
K861315 HYPERBARIC PENETRATION EXTENSION SET
K854106 BAYSILEX
K842324 PERFOURM
K832237 ORTHOPEDIC CASTING TAPE MAXCAST
K823214 DOSIMETRIC RELEASE PROGRAM - ADMIN. SET
K821326 CUTTER BOND POLYCARBOXYLATE CEMENT
K813532 CUTTERBOND ZINC PHOSPHATE CEMENT
K802105 C-BLADE
K802104 C-SPLINT
K801652 TOTAL PARENTERAL NUTRITION SET BAG
Search all 39 clearances from Cutter Laboratories, Inc. →