Go Medical Industries Pty. , Ltd.

11 FDA 510(k) medical device clearances.

Top product codes for Go Medical Industries Pty. , Ltd.

FCM — Gastroenterology, Urology 2 devices
GDM — General, Plastic Surgery 2 devices
HDB — Obstetrics/Gynecology 2 devices
FPA — General Hospital 1 device
FRN — General Hospital 1 device
HGE — Obstetrics/Gynecology 1 device
KOD — Gastroenterology, Urology 1 device
MEB — General Hospital 1 device

Recent clearances by Go Medical Industries Pty. , Ltd.

K011055 — THE O'NEIL STERILE FIELD URINARY CATHETER KIT WITH PREP PADS FCM · 2001-06-06
K002803 — THE O'NEIL STERILE FIELD URINARY CATHETER KIT FCM · 2000-12-27
K000263 — GO MEDICAL BALLOON INFUSION SYSTEM MEB · 2000-05-09
K910007 — SPRINGFUSOR 10R FRN · 1993-11-02
K900336 — V SET FPA · 1990-10-04
K895594 — SINGLE LUMEN O'NEIL ASPIRATION & IRRIGATION NEEDLE GDM · 1989-10-06
K890400 — MODIFIED URINARY CATHETER INTRODUCER (UCI) KOD · 1989-09-12
K891465 — OBSTETRIC CUP (MODIFICATION) HDB · 1989-05-11
K885283 — ASPIRATING AND IRRIGATING CYSTS NEEDLES GDM · 1989-03-22
K850758 — AMNIGLOVE & AMNICOT HGE · 1985-04-15
K840008 — O'NEIL OBSTETRIC CUP HDB · 1984-04-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.