Itl Corporation Pty, Ltd. is one of 4782 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Itl Corporation Pty, Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Itl Corporation Pty, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 5 cleared submissions from 1999 to 2016. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Itl Corporation Pty, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Itl Corporation Pty, Ltd.
5 devices
Cleared
Jun 23, 2016
Quiver Laparoscopic Extendable
General & Plastic Surgery
204d
Cleared
Jul 02, 2002
SAMPLOK LUER KIT
Chemistry
19d
Cleared
Jun 19, 2002
LEESPEC DISPOSABLE VAGINAL SPECULUM
Obstetrics & Gynecology
82d
Cleared
Apr 11, 2000
SAMPLOK
Chemistry
33d
Cleared
May 14, 1999
PLATYPUS AV FISTULA NEEDLE PROTECTOR (AVFNP)
General Hospital
22d