Medical Device Manufacturer · US , Minneapolis , MN

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

42 submissions · 37 cleared · Since 1996

Total

Cleared

Denied

Nellcor Puritan Bennett, Inc. has 37 FDA 510(k) cleared anesthesiology devices. Based in Minneapolis, US.

Historical record: 37 cleared submissions from 1996 to 2007.

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 Puritan Bennett, Inc.

42 devices

1-12 of 42

Cleared May 25, 2007

DURAMAX REUSABLE OXIMETRY SENSOR

K070408 · DQA

Anesthesiology · 102d

Cleared Aug 14, 2006

NELLCOR OXIMAX N-600X PULSE OXIMETER

K060576 · DQA

Anesthesiology · 161d

Cleared Jan 10, 2006

OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSOR

K051271 · DQA

Anesthesiology · 238d

Cleared Nov 10, 2005

NELLCOR OXIMAX PULSE OXIMETRY SENSONS (MAX-A, MAX-AL, MAX-N, MAX-I, MAX-P

K052186 · DQA

Anesthesiology · 91d

Cleared Aug 11, 2005

OXIMAX NPB-40 HANDHELD PULSE OXIMETER

Anesthesiology · 152d

Cleared Dec 13, 2004

OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR

K033973 · NLF

Anesthesiology · 357d

Cleared Nov 14, 2003

SHILEY FLEXTRA TRACHEOSTOMY TUBE

K030787 · JOH

Anesthesiology · 247d

Cleared May 23, 2003

OXIMAX SOFTCARE SENSORS, MODELS SC-A, SC-PR, SC-NEO, SC-N

K030930 · DQA

Anesthesiology · 59d

Cleared Feb 07, 2003

NELLCOR INDGO MANUAL RESUSCITATOR

K023494 · BTM

Anesthesiology · 112d

Cleared Sep 24, 2002

NELLCOR N-200 PULSE OXIMETER, MODEL N-200

K022819 · DQA

Anesthesiology · 29d

Cleared Aug 07, 2002

800 SERIES EASYNEB NEBULIZER

K020357 · CAF

Anesthesiology · 184d

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

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