# Go Medical Industries Pty., Ltd.

- Location (FDA's records): Subiaco, Perth, AU
- FDA decisions: 11 (1984–2001): 11 510(k) clearances
- Product codes: HDB (2), FCM (2), GDM (2), FRN (1), MEB (1), FPA (1), HGE (1), KOD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K011055: The O'neil Sterile Field Urinary Catheter Kit with Prep Pads (Jun 6, 2001)
- K002803: The O'neil Sterile Field Urinary Catheter Kit (Dec 27, 2000)
- K000263: GO Medical Balloon Infusion System (May 9, 2000)
- K910007: Springfusor 10R (Nov 2, 1993)
- K900336: V SET (Oct 4, 1990)
- K895594: Single Lumen O'neil Aspiration & Irrigation Needle (Oct 6, 1989)
- K890400: Modified Urinary Catheter Introducer (Uci) (Sep 12, 1989)
- K891465: Obstetric Cup (Modification) (May 11, 1989)

Source page: https://510kreport.com/company/go-medical-industries