Migada, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K954883FREE FLOW SAFETY DEVICEApril 23, 1996
K943095IV TRANSFER SPIKESeptember 30, 1994
K933929LAB-SITE(R) SAFETY CANNULADecember 7, 1993
K902881LAB-SITE SAFETY NEEDLESeptember 26, 1990
K870016ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)May 28, 1987
K864453EMERGENCY & MILITARY INFUSION SYSTEMJanuary 20, 1987
K863304PRESELECTED FLOW RATE I.V. SETDecember 9, 1986
K860952I.V. SET WITH AND WITHOUT AIR VENTAugust 27, 1986
K861275HIGH FLOW I.V. SETJune 2, 1986
K860595TRANSFER SETApril 7, 1986
K860605FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTERMarch 24, 1986
K854365IV SETS WITH NO PHTHALATE PLASTICIZER COMPONENTSMarch 24, 1986
K860201PARENTERAL ADMINISTRATION SETFebruary 4, 1986
K853385I.A.S.S., IV SET W/AIR VENT & I.A.P.S. W/O AIRVENTAugust 23, 1985
K853386MULTISET 40August 22, 1985
K853387ET - EXTENSION SETSAugust 22, 1985