FDA 510(k) Applications Submitted by HOWARD BAILIN
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K050194 |
01/27/2005 |
AXON SYSTEMS SUBDERMAL NEEDLE ELECTRODES |
AXON SYSTEMS, INC. |
K010697 |
03/08/2001 |
UNIQUE AMBULATORY EEG |
AXON SYSTEMS, INC. |
K090838 |
03/27/2009 |
STIMULUS/DISSECTION INSTRUMENTS |
AXON SYSTEMS, INC. |
K050798 |
03/29/2005 |
ECLIPSE NEUROLOGICAL WORKSTATION |
AXON SYSTEMS, INC. |
K061113 |
04/21/2006 |
ORTHOMON |
AXON SYSTEMS, INC. |
K971819 |
05/16/1997 |
EPOCH 2000 NEUROLOGICAL WORKSTATION |
AXON SYSTEMS, INC. |
K061639 |
06/12/2006 |
ECLIPSE TCD NEUROVASCULAR WORKSTATION; ELCLIPSE NEUROLOGICAL WORKSTATION WITH TCD AND VASCULAR DOPPLER; CARDIOMON |
AXON SYSTEMS, INC. |
K002316 |
07/31/2000 |
PHOENIX DIGITAL EEG |
AXON SYSTEMS, INC. |
K062198 |
08/01/2006 |
SUNSPOTS PRE-GELLED SURFACE ELECTRODES |
AXON SYSTEMS, INC. |
K022785 |
08/22/2002 |
EPOCH XP NEUROLOGICAL WORKSTATION; EPOCH XP LITE NEUROLOGICAL WORKSTATION |
AXON SYSTEMS, INC. |
K032741 |
09/04/2003 |
EPOCHXP NEUROLOGICAL WORKSTATION,EPOCHXP LITE NEUROLOGICAL WORKSTATION |
AXON SYSTEMS, INC. |
K062996 |
10/02/2006 |
DISPOSABLE MONOPOLAR AND BIPOLAR STIMULATOR PROBES |
AXON SYSTEMS, INC. |
K955257 |
11/07/1995 |
SS102 DUAL CHANNEL SEP STIMULATOR |
AXON SYSTEMS, INC. |
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