Med-West, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K880877CONTRAST INJECTION DEVICEMay 31, 1988
K880398POWER TOILET ELEVATORMarch 17, 1988
K874470MWI 400 WOUND DRESSINGDecember 18, 1987
K872724SHEATH/DILATORSSeptember 15, 1987
K854612ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7January 3, 1986
K852162MNI 400 INJECTION CAPSJune 12, 1985
K842342MWI 888 & 666 DOUBLE LUMEN SUBCLAVIANJune 14, 1984
K832124CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPIAugust 12, 1983
K831828TEFLON FEMORAL CATHETER MWI 100,10 &July 7, 1983
K831401SINGLE NEEDLE SUBCLAVIAN VEIN ACCESSJune 3, 1983
K831440SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260June 3, 1983