Go Medical Industries Pty. , Ltd.

Go Medical Industries Pty. , Ltd. holds 11 FDA 510(k) medical device clearances, first cleared 1984, most recent 2001.

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

FCM — Gastroenterology, Urology2 devices
GDM — General, Plastic Surgery2 devices
HDB — Obstetrics/Gynecology2 devices
FPA — General Hospital1 device
FRN — General Hospital1 device
HGE — Obstetrics/Gynecology1 device
KOD — Gastroenterology, Urology1 device
MEB — General Hospital1 device

Recent clearances by Go Medical Industries Pty. , Ltd.

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

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