Ivac 280 Volumetric Infusion Controller

FDA 510(k) K842419 · Y

Substantially Equivalent

510(k) numberK842419

Submission

Device name
Ivac 280 Volumetric Infusion Controller
Applicant
Y
Mchenry, IL, US
Received
June 20, 1984
Decision date
August 7, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LDR – Controller, Infusion, Intravascular, Electronic
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

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K934095Ivac Vented Syringe Adapter Administration SetsFPA · Traditional 08/10/1994SE
K940897Ivac Needleless Infection Valve Administration SetFPA · Traditional 06/22/1994SE
K931550Ez Administration SetFPA · Traditional 01/10/1994SE
K932544Ivac Space Saver Volumetric Pump, Model 599FRN · Traditional 10/12/1993SE
K931549Model EZ-1 Sing CHAN/EZ-2 Dual Channel Infus PumpFRN · Traditional 10/12/1993SE
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Questions and answers

When was Ivac 280 Volumetric Infusion Controller cleared by the FDA?

Ivac 280 Volumetric Infusion Controller (K842419) received a 510(k) decision of Substantially Equivalent on August 7, 1984, 48 days after the submission was received.

What is the product code of K842419?

The FDA product code is LDR – Controller, Infusion, Intravascular, Electronic, a Class II (moderate risk) device regulated under 21 CFR 880.5725.