# P.T. Greenleaf

- Location (FDA's records): Perth, AU
- FDA decisions: 2 (2003–2003): 2 510(k) clearances
- Product codes: FPA (1), MEA (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K020419: V SET (Aug 29, 2003)
- K020418: GO Medical Patient Controlled Analgesia Devices (Apr 29, 2003)

Source page: https://510kreport.com/company/pt-greenleaf
