Axon Systems, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Axon Systems, Inc. has 15 FDA 510(k) cleared neurology devices. Based in Deer Park, US.
Historical record: 15 cleared submissions from 1986 to 2009.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Jul 20, 2009
STIMULUS/DISSECTION INSTRUMENTS
Ear, Nose, Throat
115d
Cleared
Jan 12, 2007
DISPOSABLE MONOPOLAR AND BIPOLAR STIMULATOR PROBES
Neurology
102d
Cleared
Dec 19, 2006
SUNSPOTS PRE-GELLED SURFACE ELECTRODES
Neurology
140d
Cleared
Nov 01, 2006
ECLIPSE TCD NEUROVASCULAR WORKSTATION
Radiology
142d
Cleared
May 23, 2006
ORTHOMON
Neurology
32d
Cleared
Aug 15, 2005
ECLIPSE NEUROLOGICAL WORKSTATION
Neurology
139d
Cleared
Apr 26, 2005
AXON SYSTEMS SUBDERMAL NEEDLE ELECTRODES
Neurology
89d
Cleared
Dec 16, 2003
EPOCHXP NEUROLOGICAL WORKSTATION,EPOCHXP LITE NEUROLOGICAL WORKSTATION
Neurology
103d
Cleared
Oct 09, 2002
EPOCH XP NEUROLOGICAL WORKSTATION
Neurology
48d
Cleared
Jun 06, 2001
UNIQUE AMBULATORY EEG
Neurology
90d
Cleared
Oct 26, 2000
PHOENIX DIGITAL EEG
Neurology
87d
Cleared
Nov 20, 1997
EPOCH 2000 NEUROLOGICAL WORKSTATION
Neurology
188d
Cleared
Feb 02, 1996
SS102 DUAL CHANNEL SEP STIMULATOR
Neurology
87d
Cleared
Jun 20, 1990
SOFTWARE & HARDWARE ADDITION TO SENTINEL-4 EEG
Neurology
139d
Cleared
Dec 02, 1986
SENTINEL 4 EEG ANALYZER
Neurology
105d