Medical Device Manufacturer · IL , Israel

Migada, Ltd. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1985

Total

Cleared

Denied

Migada, Ltd. has 15 FDA 510(k) cleared general hospital devices. Based in Israel, IL.

Historical record: 15 cleared submissions from 1985 to 1994.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Migada, Ltd.

15 devices

1-12 of 15

Cleared Sep 30, 1994

IV TRANSFER SPIKE

K943095 · LHI

General Hospital · 94d

Cleared Dec 07, 1993

LAB-SITE(R) SAFETY CANNULA

K933929 · CBF

Anesthesiology · 119d

Cleared Sep 26, 1990

LAB-SITE SAFETY NEEDLE

K902881 · CBT

Anesthesiology · 86d

Cleared May 28, 1987

ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)

K870016 · DTB

Cardiovascular · 146d

Cleared Jan 20, 1987

EMERGENCY & MILITARY INFUSION SYSTEM

K864453 · FPA

General Hospital · 69d

Cleared Dec 09, 1986

PRESELECTED FLOW RATE I.V. SET

K863304 · FPA

General Hospital · 106d

Cleared Aug 27, 1986

I.V. SET WITH AND WITHOUT AIR VENT

K860952 · FPA

General Hospital · 167d

Cleared Jun 02, 1986

HIGH FLOW I.V. SET

K861275 · FPA

General Hospital · 56d

Cleared Apr 07, 1986

TRANSFER SET

K860595 · LHI

General Hospital · 47d

Cleared Mar 24, 1986

IV SETS WITH NO PHTHALATE PLASTICIZER COMPONENTS

K854365 · FPA

General Hospital · 146d

Cleared Mar 24, 1986

FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER

K860605 · FPA

General Hospital · 33d

Cleared Feb 04, 1986

PARENTERAL ADMINISTRATION SET

K860201 · FPA

General Hospital · 13d

Migada, Ltd. - FDA 510(k) Cleared Devices

Filters