Gil-Med Industries C/O Kegan & Kegan, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gil-Med Industries C/O Kegan & Kegan, Ltd. - FDA 510(k) Cleared Devic...
7
Total
7
Cleared
0
Denied
Gil-Med Industries C/O Kegan & Kegan, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1984 to 1988. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gil-Med Industries C/O Kegan & Kegan, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gil-Med Industries C/O Kegan & Kegan, Ltd.
7 devices
Cleared
May 20, 1988
MODIFIED EVA-MIX AND DI-MIX BAGS
General Hospital
102d
Cleared
Feb 10, 1987
DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER
General Hospital
14d
Cleared
Aug 11, 1986
DIETO CONTAINER FOR ENTERAL NUTRITION
Gastroenterology & Urology
90d
Cleared
Oct 26, 1984
GIL-MED PARENTERAL NUTRITION OR MEDICINE
General Hospital
191d
Cleared
May 02, 1984
URO-MALE INCONTINENCE CATHETER
Gastroenterology & Urology
41d
Cleared
Apr 17, 1984
DIMIX CONTAINER FOR PARNETERAL NUTRIT
General Hospital
48d
Cleared
Apr 04, 1984
DIETO CONTAINER FOR ENTERNAL NUTRIT
Gastroenterology & Urology
35d