# Fisher & Paykel Allied Products, Ltd.

- Location (FDA's records): Auckland, New Zealand, NZ
- FDA decisions: 12 (1982–1988): 12 510(k) clearances
- Product codes: BTT (11), BXN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Intersurgical, Inc.: 2 (https://510kreport.com/company/intersurgical)
- Marquest Medical Products, Inc.: 2 (https://510kreport.com/company/marquest-medical-products)
- I.P.I. Medical Products: 2 (https://510kreport.com/company/ipi-medical-products)

## Its most-cited devices
- K862923: MR620 Dual Servo Heated Anaesthesia Humidifier (1986), cited by 3
- K850647: Heated Respiratory Humififier MR440 (1985), cited by 3

## Recent decisions
- K880702: Model MR430 Special Purpose Humid. Heater Bases (Jul 8, 1988)
- K872138: MR630 Enhanced Dual Servo Heater Humidifier (Oct 7, 1987)
- K872139: MR420 Transport Humidifier (Sep 15, 1987)
- K863377: MR338 Servo Heated Delivery Humidifier (Feb 20, 1987)
- K870055: MR590 Dual Hose Heater Power Pack (Feb 10, 1987)
- K862923: MR620 Dual Servo Heated Anaesthesia Humidifier (Sep 23, 1986)
- K852962: Peripheral Nerve Stimulator Model A400 (Dec 9, 1985)
- K851879: Heated Respiratory Humidifier (Sep 3, 1985)

Source page: https://510kreport.com/company/fisher-paykel-allied-products