Medical Device Manufacturer · US , Mchenry , IL

Nellcor, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1982

Total

Cleared

Denied

Nellcor, Inc. has 18 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1982 to 1995.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Nellcor, Inc.

18 devices

1-12 of 18

Cleared Oct 20, 1995

NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOR

K953472 · DXN

Cardiovascular · 88d

Cleared Aug 17, 1995

NELLCOR SYMPHONY N-3000 PULSE OXIMETER

K952316 · DQA

Anesthesiology · 92d

Cleared Aug 15, 1995

NELLCOR N-20PA PORTABLE PULSE OXIMETER

K952222 · DQA

Anesthesiology · 95d

Cleared May 12, 1995

NELLCOR SYMPHONY PULSE OXIMETER MODEL N-3000

K942347 · DQA

Anesthesiology · 360d

Cleared Mar 08, 1995

NELLCOR SYMPHONY(TM) N-3100 BLOOD PRESSURE MONITOR AND CONNECTED TO THE...

K945947 · DXN

Cardiovascular · 92d

Cleared Oct 17, 1994

DURA-Y OXYGEN TRANSDUCER, EAR CLIP

NELLCOR STAT-CAP AIRWAY CO2 INDICATOR, MODEL N-60

K915494 · CCK

Anesthesiology · 606d

Cleared May 27, 1993

NELLCOR PORTABLE PULSE OXIMETER MODEL N-20

K915699 · DQA

Anesthesiology · 521d

Cleared Nov 13, 1991

NELLCOR(R) N-180 PULSE OXIMETER

K913695 · DQA

Anesthesiology · 86d

Cleared Dec 27, 1990

REFLECTANCE SENSOR (RS-10)

K904039 · DQA

Anesthesiology · 114d

Nellcor, Inc. - FDA 510(k) Cleared Devices

Filters