Natus Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Natus Medical, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Natus Medical, Inc. has 12 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Historical record: 12 cleared submissions from 1995 to 2010. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Natus Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Natus Medical, Inc.
12 devices
Cleared
Aug 11, 2010
PROTEKTOR 32
Neurology
294d
Cleared
Jun 16, 2010
OLYMPIC BRAINZ MONITOR MODEL OBM70001
Neurology
175d
Cleared
Feb 22, 2010
NATUS NEUROWORKS, MODEL 104196
Neurology
416d
Cleared
Dec 08, 2009
NAVIGATOR PRO WITH AEP SOFTWARE (BIOMARK, ENOG, CHAMP)
Neurology
389d
Cleared
Jan 25, 2008
ALGO 5 NEWBORN HEARING SCREENER
Neurology
30d
Cleared
Oct 07, 2005
NEOBLUE COZY LED PHOTOTHERAPY SYSTEM
General Hospital
88d
Cleared
Apr 09, 2003
ALGO 3I NEWBORN HEARING SCREENER
Neurology
26d
Cleared
Sep 19, 2002
NATUS BLUE LIGHT PHOTOTHERAPY UNIT
General Hospital
76d
Cleared
Oct 16, 2001
ALGO 3 NEWBORN HEARING SCREENER
Neurology
27d
Cleared
Mar 11, 1998
CO-STAT(TM) END TIDAL BREATH ANALYZER
Hematology
78d
Cleared
Feb 09, 1995
MINIMUFFS
Ear, Nose, Throat
468d
Cleared
Jan 05, 1995
ALGO-2 NEWBORN HEARING SCREENER
Neurology
381d