Imed Corp. - FDA 510(k) Cleared Devices
43
Total
43
Cleared
0
Denied
Imed Corp. has 43 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.
Historical record: 43 cleared submissions from 1977 to 1996.
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 - Imed Corp.
43 devices
Cleared
Nov 21, 1996
GEMINI PC-ITX
General Hospital
290d
Cleared
Mar 20, 1996
THE IMED AMBULATORY INFUSION PUMP, ADMINISTRATION SETS
General Hospital
216d
Cleared
Aug 24, 1995
VENTED/NONVENTED GEMINI ADMINISTRATION SET WITH CHECK VALVE AND TWO...
General Hospital
219d
Cleared
Jul 19, 1995
ADMINISTRATION SETS WITH BALL FLOAT
General Hospital
86d
Cleared
Jun 21, 1995
THE IMED ORION INFUSION PUMP AND ADMINISTRATION SETS
General Hospital
141d
Cleared
Feb 14, 1995
VENTED/NON-VENTED GEMINI ADMINISTRATION SET
General Hospital
169d
Cleared
Jan 13, 1995
VERSASAE PLASTIC CANNULA- 11 GAUGE
General Hospital
91d
Cleared
Apr 15, 1994
PRIMARY ADMIN SET W/UNIV SP-MAN BELOW/ABV PUMP CH
General Hospital
403d
Cleared
Oct 12, 1993
GEMINI VOLUMETRIC INFUSION PUMP/CONTROLLER
General Hospital
106d
Cleared
Jun 18, 1993
SHROUDED NEEDLE DEVICES
General Hospital
270d
Cleared
Jun 09, 1992
IMED MODEL PC-4 VOLUMETRIC INFUSION PUMP/CONTROLLE
General Hospital
78d
Cleared
Mar 26, 1992
IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD
General Hospital
241d
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