Fisher & Paykel Electronics , Ltd.
Fisher & Paykel Electronics , Ltd. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1998.
Top product codes for Fisher & Paykel Electronics , Ltd.
Recent clearances by Fisher & Paykel Electronics , Ltd.
- K973161 — CPAP HUMIDIFIER (HC 200)
- K972885 — SERVO-CONTROL WALL-MOUNT COSYCOT INFANT WARMER MODEL IW960, MANUAL CONTROL WALL-MOUNT COSYCOT INFANT WARMER MODEL IW970
- K971695 — SERVO-CONTROL COSYCOT INFANT WARMER, MANUAL-CONTROL COSYCOT INFANT WARMER
- K971461 — SERVO-CONTROL WALL-MOUNT INFANT WARMER(IW980)/MANUAL-CONTROL WALL-MOUNT INFANT WARMER(IW990)
- K970432 — INFANT RADIANT WARMER - MODELS IW910 AND IW920
- K953392 — HC500 SERVO-CONTROLLED HEATED RESPIRATORY HUMIDIFIER (& ACCESSORIES)
- K953711 — AIR ENTRAINER 900RT008
- K953949 — HUMIDIFIER & ACCESSORIES
- K934140 — MR290 HUMIDIFICATION CHAMBER SINGLE USE
- K924234 — CONS. CURRENT PERIPH. NERVE LOC. NS232,NS262,NS272
- K915460 — HEATED RESPIRATORY HUMIDIFIER HC100
- K913367 — MODELS MR410 & MR480 RESPIRATORY HUMIDIFIER/ACCESS
- K902386 — MODEL TM101 TEMPERATURE MONITOR
- K913368 — MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC
- K892817 — HEATED RESPIRATORY HUMIDIFIER
- K892885 — RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR
- K883868 — MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM
Data sourced from openFDA. This site is unofficial and independent of the FDA.