Exel Intl. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - Exel Intl. General Hospital ✕
13 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
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
Sep 25, 1986
EXEL THREE-WAY STOPCOCK
General Hospital
86d
Cleared
Aug 27, 1986
EXEL BUTTERFLY SCALP VEIN SET
General Hospital
57d
Cleared
May 06, 1986
EXEL VACUUM BLOOD COLLECTING SYSTEM
General Hospital
41d
Cleared
Apr 23, 1986
DISPOSABLE SYRINGES AND HYPODERMIC NEEDLES
General Hospital
28d