Nellcor Puritan Bennett, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nellcor Puritan Bennett, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DURAMAX REUSABLE OXIMETRY SENSOR, NELLCOR OXIMAX N-600X PULSE OXIMETER, OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSOR
42
Total
37
Cleared
0
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
Cleared
May 25, 2007
DURAMAX REUSABLE OXIMETRY SENSOR
Anesthesiology
102d
Cleared
Aug 14, 2006
NELLCOR OXIMAX N-600X PULSE OXIMETER
Anesthesiology
161d
Cleared
Jan 10, 2006
OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSOR
Anesthesiology
238d
Cleared
Nov 10, 2005
NELLCOR OXIMAX PULSE OXIMETRY SENSONS (MAX-A, MAX-AL, MAX-N, MAX-I, MAX-P
Anesthesiology
91d
Cleared
Aug 11, 2005
OXIMAX NPB-40 HANDHELD PULSE OXIMETER
Anesthesiology
79d
Cleared
Jun 13, 2005
GOODKNIGHT 425ST
Anesthesiology
152d
Cleared
Dec 13, 2004
OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR
Anesthesiology
357d
Cleared
Nov 14, 2003
SHILEY FLEXTRA TRACHEOSTOMY TUBE
Anesthesiology
247d
Cleared
May 23, 2003
OXIMAX SOFTCARE SENSORS, MODELS SC-A, SC-PR, SC-NEO, SC-N
Anesthesiology
59d
Cleared
Feb 07, 2003
NELLCOR INDGO MANUAL RESUSCITATOR
Anesthesiology
112d
Cleared
Sep 24, 2002
NELLCOR N-200 PULSE OXIMETER, MODEL N-200
Anesthesiology
29d
Cleared
Aug 07, 2002
800 SERIES EASYNEB NEBULIZER
Anesthesiology
184d
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