Nellcor, Inc.
Nellcor, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1995.
Top product codes for Nellcor, Inc.
Recent clearances by Nellcor, Inc.
- K953472 — NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOR
- K952316 — NELLCOR SYMPHONY N-3000 PULSE OXIMETER
- K952222 — NELLCOR N-20PA PORTABLE PULSE OXIMETER
- K942347 — NELLCOR SYMPHONY PULSE OXIMETER MODEL N-3000
- K945947 — NELLCOR SYMPHONY(TM) N-3100 BLOOD PRESSURE MONITOR AND CONNECTED TO THE NELLCOR SYMPHONY(TM) N-3000 PULSE OXIMETER
- K944760 — DURA-Y OXYGEN TRANSDUCER, EAR CLIP
- K944400 — PEDI-CAP
- K915494 — NELLCOR STAT-CAP AIRWAY CO2 INDICATOR, MODEL N-60
- K915699 — NELLCOR PORTABLE PULSE OXIMETER MODEL N-20
- K913695 — NELLCOR(R) N-180 PULSE OXIMETER
- K904039 — REFLECTANCE SENSOR (RS-10)
- K901399 — POWERBASE II (PB2)
- K896629 — NELLCOR MODEL N-2500 ANESTHESIA SAFETY MONITOR
- K884142 — OXINET N-7500 PULSE OXIMETRY NETWORK
- K862812 — NELLCOR MVP, MODEL N-1000
- K863784 — NELLCOR N-200 (PULSE OXIMETER)
- K844256 — NELLCOR PULSE OXIMETER N-10
- K822909 — PULSE OXIMETER MODEL 100
Data sourced from openFDA. This site is unofficial and independent of the FDA.