Deseret Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K913027VESSEL DILATORNovember 27, 1991
K904648SAFE SYTE I.V. CATHETER PLACEMENT UNITDecember 14, 1990
K904121VIALON OBTURATORNovember 8, 1990
K904122INSYTE-A ARTERIAL CATHETERIZATION UNITOctober 4, 1990
K900116DESERET OPTIMA INTRAVASCULAR CATHETERJune 18, 1990
K895735DESERET MULTILUMEN SUBCLAVIAN CATHETERMay 18, 1990
K895734DESERET INTRAVASCULAR CATHETERApril 9, 1990
K894033DISPOSABLE CATHETER PRESSURE TRANSDUCEROctober 17, 1989
K893406DESERET PRN ADAPTERJune 22, 1989
K882797LUER-LOK MULTIFLO ADAPTERJuly 18, 1988
K882798MULTIFLO ADAPTERJuly 18, 1988
K881695DESERET SUBCLAVIAN HEMODIALYSIS CATHETERJune 23, 1988
K874165DISPOSABLE CATHETER PRESSURE TRANSDUCERJune 9, 1988
K874582DESERET SPLITTABLE CATHETERDecember 29, 1987
K833657ANGIO-SET INTRAVENOUS CATH. SETDecember 27, 1983
K832558RELEASE OF ETHYLENE OXIDE-STERILIZ. DEVNovember 28, 1983
K813595PARKE-DAVIS AEGIS ABOSRBENT SPONGESJanuary 18, 1982
K811343HUMERAL FRACTURE CAST BRACEMay 28, 1981
K801650DESERET EMBOLECTOMY/THROMBECTOMY CATH.August 4, 1980
K790327ANGIO-FLOFebruary 26, 1979