Axon Systems, Inc.
FDA 510(k) & PMA Approved Devices — 15 products
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Total Devices15
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K090838 | STIMULUS/DISSECTION INSTRUMENTS | ETN | 2009-07-20 | View |
| 510(k) | K062996 | DISPOSABLE MONOPOLAR AND BIPOLAR STIMULATOR PROBES | GXZ | 2007-01-12 | View |
| 510(k) | K062198 | SUNSPOTS PRE-GELLED SURFACE ELECTRODES | GXY | 2006-12-19 | View |
| 510(k) | K061639 | ECLIPSE TCD NEUROVASCULAR WORKSTATION; ELCLIPSE NEUROLOGICAL WORKSTATION WITH TCD AND VASCULAR DOPPLER; CARDIOMON | GWF | 2006-11-01 | View |
| 510(k) | K061113 | ORTHOMON | GWF | 2006-05-23 | View |
| 510(k) | K050798 | ECLIPSE NEUROLOGICAL WORKSTATION | GWF | 2005-08-15 | View |
| 510(k) | K050194 | AXON SYSTEMS SUBDERMAL NEEDLE ELECTRODES | GXZ | 2005-04-26 | View |
| 510(k) | K032741 | EPOCHXP NEUROLOGICAL WORKSTATION,EPOCHXP LITE NEUROLOGICAL WORKSTATION | GWF | 2003-12-16 | View |
| 510(k) | K022785 | EPOCH XP NEUROLOGICAL WORKSTATION; EPOCH XP LITE NEUROLOGICAL WORKSTATION | GWQ | 2002-10-09 | View |
| 510(k) | K010697 | UNIQUE AMBULATORY EEG | GWQ | 2001-06-06 | View |
| 510(k) | K002316 | PHOENIX DIGITAL EEG | GWQ | 2000-10-26 | View |
| 510(k) | K971819 | EPOCH 2000 NEUROLOGICAL WORKSTATION | GWF | 1997-11-20 | View |
| 510(k) | K955257 | SS102 DUAL CHANNEL SEP STIMULATOR | GWF | 1996-02-02 | View |
| 510(k) | K900482 | SOFTWARE & HARDWARE ADDITION TO SENTINEL-4 EEG | GWF | 1990-06-20 | View |
| 510(k) | K863193 | SENTINEL 4 EEG ANALYZER | GWQ | 1986-12-02 | View |
No matching devices.
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