FDA 510(k) Applications Submitted by AXON SYSTEMS, INC.

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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