Nellcor, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K953472NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOROctober 20, 1995
K952316NELLCOR SYMPHONY N-3000 PULSE OXIMETERAugust 17, 1995
K952222NELLCOR N-20PA PORTABLE PULSE OXIMETERAugust 15, 1995
K942347NELLCOR SYMPHONY PULSE OXIMETER MODEL N-3000May 12, 1995
K945947NELLCOR SYMPHONY(TM) N-3100 BLOOD PRESSURE MONITOR AND CONNECTED TO THE NELLCOR SYMPHONY(TM) N-3000 March 8, 1995
K944760DURA-Y OXYGEN TRANSDUCER, EAR CLIPOctober 17, 1994
K944400PEDI-CAPSeptember 27, 1994
K915494NELLCOR STAT-CAP AIRWAY CO2 INDICATOR, MODEL N-60August 6, 1993
K915699NELLCOR PORTABLE PULSE OXIMETER MODEL N-20May 27, 1993
K913695NELLCOR(R) N-180 PULSE OXIMETERNovember 13, 1991
K904039REFLECTANCE SENSOR (RS-10)December 27, 1990
K901399POWERBASE II (PB2)June 12, 1990
K896629NELLCOR MODEL N-2500 ANESTHESIA SAFETY MONITORFebruary 12, 1990
K884142OXINET N-7500 PULSE OXIMETRY NETWORKDecember 16, 1988
K862812NELLCOR MVP, MODEL N-1000December 22, 1986
K863784NELLCOR N-200 (PULSE OXIMETER)November 21, 1986
K844256NELLCOR PULSE OXIMETER N-10December 27, 1984
K822909PULSE OXIMETER MODEL 100November 1, 1982