Fisher & Paykel Allied Products , Ltd.

Fisher & Paykel Allied Products , Ltd. holds 12 FDA 510(k) medical device clearances, first cleared 1982, most recent 1988.

Top product codes for Fisher & Paykel Allied Products , Ltd.

BTT — Anesthesiology11 devices
BXN — Anesthesiology1 device

Recent clearances by Fisher & Paykel Allied Products , Ltd.

K880702 — MODEL MR430 SPECIAL PURPOSE HUMID. HEATER BASESCode BTT·1988-07-08
K872138 — MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIERCode BTT·1987-10-07
K872139 — MR420 TRANSPORT HUMIDIFIERCode BTT·1987-09-15
K863377 — MR338 SERVO HEATED DELIVERY HUMIDIFIERCode BTT·1987-02-20
K870055 — MR590 DUAL HOSE HEATER POWER PACKCode BTT·1987-02-10
K862923 — MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIERCode BTT·1986-09-23
K852962 — PERIPHERAL NERVE STIMULATOR MODEL A400Code BXN·1985-12-09
K851879 — HEATED RESPIRATORY HUMIDIFIERCode BTT·1985-09-03
K850647 — HEATED RESPIRATORY HUMIFIFIER MR440Code BTT·1985-03-12
K843903 — HEATED RESPIRATORY HUMIDIFIER MR428Code BTT·1984-10-22
K832928 — SERVO HEATED RESPIRATORY HUMIDIFIERCode BTT·1983-11-25
K822816 — DUAL SERVO HEATED RESPIRATORY HUMIDIFIERCode BTT·1982-10-22

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