Exel Intl. is one of 13820 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Exel Intl. - FDA 510(k) Cleared Devices
Recent clearances: EXEL INJECTION PLUG WITH CAP, EXEL AVF SINGLE NEEDLE, EXEL I.V. ADMINISTRATION SET
18
Total
18
Cleared
0
Denied
Exel Intl. has 18 FDA 510(k) cleared general hospital devices. Based in Culver City, US.
Historical record: 18 cleared submissions from 1986 to 2000.
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 - Exel Intl.
18 devices
Cleared
Feb 23, 2000
EXEL INJECTION PLUG WITH CAP
General Hospital
231d
Cleared
May 05, 1998
EXEL AVF SINGLE NEEDLE
General Hospital
609d
Cleared
Dec 16, 1997
EXEL I.V. ADMINISTRATION SET
General Hospital
469d
Cleared
Aug 11, 1993
EXEL HUBER INFUSION SET ROTATING WING
General Hospital
251d
Cleared
Nov 21, 1990
EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)
General Hospital
48d
Cleared
Nov 20, 1990
EXEL A-V FISTULA SET
Gastroenterology & Urology
85d
Cleared
Jul 19, 1990
EXEL HUBER INFUSION SET
General Hospital
296d
Cleared
Feb 16, 1990
EXEL SAFELET CATHETER
General Hospital
143d
Cleared
Feb 16, 1990
EXEL HUBER NEEDLE
General Hospital
143d
Cleared
Feb 16, 1990
EXEL SPINAL NEEDLES
General Hospital
143d
Cleared
Feb 16, 1990
EXEL INDWELLING CATHETER
Gastroenterology & Urology
143d
Cleared
Sep 25, 1986
EXEL THREE-WAY STOPCOCK
General Hospital
86d