Fisher & Paykel Electronics , Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Fisher & Paykel Electronics , Ltd. has 17 FDA 510(k) cleared anesthesiology devices. Based in Auckland, New Zealand, NZ.
Historical record: 17 cleared submissions from 1988 to 1998.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
17 devices
Cleared
Jul 10, 1998
CPAP HUMIDIFIER (HC 200)
Anesthesiology
322d
Cleared
Oct 30, 1997
SERVO-CONTROL WALL-MOUNT COSYCOT INFANT WARMER MODEL IW960, MANUAL CONTROL...
General Hospital
86d
Cleared
Jul 28, 1997
SERVO-CONTROL COSYCOT INFANT WARMER, MANUAL-CONTROL COSYCOT INFANT WARMER
General Hospital
81d
Cleared
Jul 16, 1997
SERVO-CONTROL WALL-MOUNT INFANT WARMER(IW980)/MANUAL-CONTROL WALL-MOUNT...
General Hospital
86d
Cleared
May 07, 1997
INFANT RADIANT WARMER - MODELS IW910 AND IW920
General Hospital
92d
Cleared
Mar 12, 1996
HC500 SERVO-CONTROLLED HEATED RESPIRATORY HUMIDIFIER (& ACCESSORIES)
Anesthesiology
237d
Cleared
Nov 08, 1995
AIR ENTRAINER 900RT008
Anesthesiology
91d
Cleared
Oct 16, 1995
HUMIDIFIER & ACCESSORIES
Anesthesiology
55d
Cleared
Jan 24, 1994
MR290 HUMIDIFICATION CHAMBER SINGLE USE
Anesthesiology
152d
Cleared
May 27, 1993
CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272
Anesthesiology
276d
Cleared
Jan 15, 1993
HEATED RESPIRATORY HUMIDIFIER HC100
Anesthesiology
408d
Cleared
Jun 25, 1992
MODELS MR410 & MR480 RESPIRATORY HUMIDIFIER/ACCESS
Anesthesiology
337d