Ivac Flow Control Administration Set

FDA 510(k) K870132 · Y

Substantially Equivalent

510(k) numberK870132

Submission

Device name
Ivac Flow Control Administration Set
Applicant
Y
San Diego, CA, US
Received
January 12, 1987
Decision date
February 5, 1987
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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More from The Master Medical Corp.

510(k)DeviceDecision
K955846Model 2082 Temp Plus III Thermometer/Model 2087 Temp Plus III Wall Mount ThermometerFLL · Traditional 10/01/1996SE
K960280Ivac Needle Free Valve Administration SetsFPA · Traditional 04/04/1996SE
K953225Ivac Ball Valce Admin. SetsFPA · Traditional 09/27/1995SE
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
K922115Ivac Needleless Injection ValveFPA · Traditional 10/12/1993SE
K930781Infusion PumpFRN · Traditional 08/19/1993SE

Questions and answers

When was Ivac Flow Control Administration Set cleared by the FDA?

Ivac Flow Control Administration Set (K870132) received a 510(k) decision of Substantially Equivalent on February 5, 1987, 24 days after the submission was received.

What is the product code of K870132?

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