Imed Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
43
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K960512GEMINI PC-ITXNovember 21, 1996
K953896THE IMED AMBULATORY INFUSION PUMP, ADMINISTRATION SETSMarch 20, 1996
K950153VENTED/NONVENTED GEMINI ADMINISTRATION SET WITH CHECK VALVE AND TWO SAFSITE(TM) VALVESAugust 24, 1995
K951922ADMINISTRATION SETS WITH BALL FLOATJuly 19, 1995
K950419THE IMED ORION INFUSION PUMP AND ADMINISTRATION SETSJune 21, 1995
K944320VENTED/NON-VENTED GEMINI ADMINISTRATION SETFebruary 14, 1995
K945070VERSASAE PLASTIC CANNULA- 11 GAUGEJanuary 13, 1995
K931173PRIMARY ADMIN SET W/UNIV SP-MAN BELOW/ABV PUMP CHApril 15, 1994
K933144GEMINI VOLUMETRIC INFUSION PUMP/CONTROLLEROctober 12, 1993
K924718SHROUDED NEEDLE DEVICESJune 18, 1993
K921378IMED MODEL PC-4 VOLUMETRIC INFUSION PUMP/CONTROLLEJune 9, 1992
K913658IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MODMarch 26, 1992
K895797IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICEJanuary 2, 1990
K894842IMED GEMINI 12 NONVENTED Y-TYPE BLOOD/SOLUTION ADMSeptember 12, 1989
K883993MODIFIED IMED GEMINI PC-1 INFUSION PUMPDecember 19, 1988
K880479IMED(R) GEMINI(TM) PC-1 VOLUMETRIC INFUSION PUMPApril 25, 1988
K870656IMED(R) 980C VOLUMETRIC INFUSION PUMPOctober 20, 1987
K872952ULTRASONIC AIR-IN-LINE DETECTOR (AILD)October 20, 1987
K870992IMED(R) MODEL 965A VOLUMETRIC INFUSION PUMPJune 4, 1987
K870991IMED(R) MODEL 960A VOLUMETRIC INFUSION PUMPJune 4, 1987