Go Medical Industries Pty. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Go Medical Industries Pty. , Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Go Medical Industries Pty. , Ltd. has 11 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 11 cleared submissions from 1984 to 2001.
Browse the FDA 510(k) cleared devices submitted by Go Medical Industries Pty. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Go Medical Industries Pty. , Ltd.
11 devices
Cleared
Jun 06, 2001
THE O'NEIL STERILE FIELD URINARY CATHETER KIT WITH PREP PADS
Gastroenterology & Urology
61d
Cleared
Dec 27, 2000
THE O'NEIL STERILE FIELD URINARY CATHETER KIT
Gastroenterology & Urology
110d
Cleared
May 09, 2000
GO MEDICAL BALLOON INFUSION SYSTEM
General Hospital
102d
Cleared
Nov 02, 1993
SPRINGFUSOR 10R
General Hospital
1035d
Cleared
Oct 04, 1990
V SET
General Hospital
254d
Cleared
Oct 06, 1989
SINGLE LUMEN O'NEIL ASPIRATION & IRRIGATION NEEDLE
General & Plastic Surgery
21d
Cleared
Sep 12, 1989
MODIFIED URINARY CATHETER INTRODUCER (UCI)
Gastroenterology & Urology
231d
Cleared
May 11, 1989
OBSTETRIC CUP (MODIFICATION)
Obstetrics & Gynecology
57d
Cleared
Mar 22, 1989
ASPIRATING AND IRRIGATING CYSTS NEEDLES
General & Plastic Surgery
92d
Cleared
Apr 15, 1985
AMNIGLOVE & AMNICOT
Obstetrics & Gynecology
49d
Cleared
Apr 25, 1984
O'NEIL OBSTETRIC CUP
Obstetrics & Gynecology
112d