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.
FDA 510(k) cleared devices by Gesco Intl., Inc.
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