Fisher & Paykel Allied Products , Ltd. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Fisher & Paykel Allied Products , Ltd. has 12 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1982 to 1988.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Jul 08, 1988
MODEL MR430 SPECIAL PURPOSE HUMID. HEATER BASES
Anesthesiology
137d
Cleared
Oct 07, 1987
MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIER
Anesthesiology
126d
Cleared
Sep 15, 1987
MR420 TRANSPORT HUMIDIFIER
Anesthesiology
105d
Cleared
Feb 20, 1987
MR338 SERVO HEATED DELIVERY HUMIDIFIER
Anesthesiology
170d
Cleared
Feb 10, 1987
MR590 DUAL HOSE HEATER POWER PACK
Anesthesiology
34d
Cleared
Sep 23, 1986
MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER
Anesthesiology
53d
Cleared
Dec 09, 1985
PERIPHERAL NERVE STIMULATOR MODEL A400
Anesthesiology
150d
Cleared
Sep 03, 1985
HEATED RESPIRATORY HUMIDIFIER
Anesthesiology
127d
Cleared
Mar 12, 1985
HEATED RESPIRATORY HUMIFIFIER MR440
Anesthesiology
21d
Cleared
Oct 22, 1984
HEATED RESPIRATORY HUMIDIFIER MR428
Anesthesiology
19d
Cleared
Nov 25, 1983
SERVO HEATED RESPIRATORY HUMIDIFIER
Anesthesiology
93d
Cleared
Oct 22, 1982
DUAL SERVO HEATED RESPIRATORY HUMIDIFIER
Anesthesiology
32d