Gesco Intl., Inc. - FDA 510(k) Cleared Devices
26
Total
22
Cleared
0
Denied
Gesco Intl., Inc. has 22 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 22 cleared submissions from 1978 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gesco Intl., Inc. Filter by specialty or product code using the sidebar.
26 devices
Cleared
Dec 15, 1995
PER-Q-CATH MID-LINE
General Hospital
85d
Cleared
Aug 02, 1994
UMBILI-CATH
General Hospital
158d
Cleared
Aug 02, 1994
UMBILI-CATH-S
General Hospital
154d
Cleared
Jul 29, 1994
UMBILI-CATH-S-DL
General Hospital
150d
Cleared
May 16, 1994
URI-CATH CATHETER
Gastroenterology & Urology
41d
Cleared
May 11, 1994
THORA-CATH
General Hospital
57d
Cleared
Apr 29, 1994
UMBILI-CATH-P
General Hospital
63d
Cleared
Jul 21, 1993
VENTRI-CATH
Neurology
90d
Cleared
Jun 07, 1993
PER-Q-CATH DRESSING CHANGE TRAY
General & Plastic Surgery
188d
Cleared
Mar 16, 1993
PALA-NATE
Anesthesiology
239d
Cleared
Jan 27, 1992
GESCO PER-Q-CATH CATHETER INTRODUCER
Cardiovascular
73d
Cleared
Aug 14, 1991
OBSTETRICAL VACUUM CUP
Obstetrics & Gynecology
141d