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Fisher & Paykel Allied Products , Ltd.

12 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODEL MR430 SPECIAL PURPOSE HUMID. HEATER BASES (K880702)Fisher & Paykel Allied Products , Ltd.1988-07-08
MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER (K872138)Fisher & Paykel Allied Products , Ltd.1987-10-07
MR420 TRANSPORT HUMIDIFIER (K872139)Fisher & Paykel Allied Products , Ltd.1987-09-15
MR338 SERVO HEATED DELIVERY HUMIDIFIER (K863377)Fisher & Paykel Allied Products , Ltd.1987-02-20
MR590 DUAL HOSE HEATER POWER PACK (K870055)Fisher & Paykel Allied Products , Ltd.1987-02-10
MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER (K862923)Fisher & Paykel Allied Products , Ltd.1986-09-23
PERIPHERAL NERVE STIMULATOR MODEL A400 (K852962)Fisher & Paykel Allied Products , Ltd.1985-12-09
HEATED RESPIRATORY HUMIDIFIER (K851879)Fisher & Paykel Allied Products , Ltd.1985-09-03
HEATED RESPIRATORY HUMIFIFIER MR440 (K850647)Fisher & Paykel Allied Products , Ltd.1985-03-12
HEATED RESPIRATORY HUMIDIFIER MR428 (K843903)Fisher & Paykel Allied Products , Ltd.1984-10-22
SERVO HEATED RESPIRATORY HUMIDIFIER (K832928)Fisher & Paykel Allied Products , Ltd.1983-11-25
DUAL SERVO HEATED RESPIRATORY HUMIDIFIER (K822816)Fisher & Paykel Allied Products , Ltd.1982-10-22

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Every clearance here is in the API, with alerts when new ones post.