Emergency & Military Infusion System

FDA 510(k) K864453 · Migada, Ltd.

Substantially Equivalent

510(k) numberK864453

Submission

Device name
Emergency & Military Infusion System
Applicant
Migada, Ltd.
Israel, IL
Received
November 12, 1986
Decision date
January 20, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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More from B.Braun Medical, Inc.

510(k)DeviceDecision
K954883Free Flow Safety DeviceFPA · Traditional 04/23/1996SE
K943095IV Transfer SpikeLHI · Traditional 09/30/1994SE
K933929Lab-Site(R) Safety CannulaCBF · Traditional 12/07/1993SE
K902881Lab-Site Safety NeedleCBT · Traditional 09/26/1990SE
K870016Arterial Blood Gassing Monitoring System (Abg)DTB · Traditional 05/28/1987SE
K863304Preselected Flow Rate I.V. SetFPA · Traditional 12/09/1986SE
K860952I.V. Set with and Without Air VentFPA · Traditional 08/27/1986SE
K861275High Flow I.V. SetFPA · Traditional 06/02/1986SE
K860595Transfer SetLHI · Traditional 04/07/1986SE
K860605Filter Set 1) 1.2 Mic Filter 2) 3.0 Mic FilterFPA · Traditional 03/24/1986SE

Questions and answers

When was Emergency & Military Infusion System cleared by the FDA?

Emergency & Military Infusion System (K864453) received a 510(k) decision of Substantially Equivalent on January 20, 1987, 69 days after the submission was received.

What is the product code of K864453?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.