Gerard Medical Enterprises, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gerard Medical Enterprises, Inc. - FDA 510(k) Cleared Devices
8
Total
6
Cleared
0
Denied
Gerard Medical Enterprises, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gerard Medical Enterprises, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gerard Medical Enterprises, Inc.
8 devices
Cleared
May 24, 1996
TRIMPORT IMPLANTABLE ACCESS SYSTEM (MODIFICATION)
General Hospital
262d
Cleared
Mar 07, 1995
TRIMPORT
General Hospital
130d
Cleared
Aug 23, 1994
TRIMPORT
General Hospital
88d
Cleared
Dec 04, 1992
DUAL PLASTIC VASCULAR ACCESS SYSTEM
General Hospital
211d
Cleared
Jan 02, 1992
TRIM-PORT(TM) IMPLANT ACCESS SYST DUAL TITAN PORT
General Hospital
178d
Cleared
Oct 08, 1991
MODIFIED VERSION IMPLANTABLE VASCULAR ACCESS SYSTE
General Hospital
148d
Cleared
Oct 31, 1990
GERARD MEDICAL, INC. TRIM-PORT
General Hospital
97d
Cleared
Dec 29, 1981
GERARD MEDICAL ELECTRODE TESTER
Cardiovascular
29d