Itl Corporation Pty, Ltd. is one of 20391 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
Recent clearances: Quiver Laparoscopic Extendable, SAMPLOK LUER KIT, LEESPEC DISPOSABLE VAGINAL SPECULUM
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.
510(k) submissions have been managed by Regulatory Resources, Inc. as regulatory consultant.
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