Axon Systems, Inc.
Axon Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2009.
Top product codes for Axon Systems, Inc.
Recent clearances by Axon Systems, Inc.
- K090838 — STIMULUS/DISSECTION INSTRUMENTS
- K062996 — DISPOSABLE MONOPOLAR AND BIPOLAR STIMULATOR PROBES
- K062198 — SUNSPOTS PRE-GELLED SURFACE ELECTRODES
- K061639 — ECLIPSE TCD NEUROVASCULAR WORKSTATION; ELCLIPSE NEUROLOGICAL WORKSTATION WITH TCD AND VASCULAR DOPPLER; CARDIOMON
- K061113 — ORTHOMON
- K050798 — ECLIPSE NEUROLOGICAL WORKSTATION
- K050194 — AXON SYSTEMS SUBDERMAL NEEDLE ELECTRODES
- K032741 — EPOCHXP NEUROLOGICAL WORKSTATION,EPOCHXP LITE NEUROLOGICAL WORKSTATION
- K022785 — EPOCH XP NEUROLOGICAL WORKSTATION; EPOCH XP LITE NEUROLOGICAL WORKSTATION
- K010697 — UNIQUE AMBULATORY EEG
- K002316 — PHOENIX DIGITAL EEG
- K971819 — EPOCH 2000 NEUROLOGICAL WORKSTATION
- K955257 — SS102 DUAL CHANNEL SEP STIMULATOR
- K900482 — SOFTWARE & HARDWARE ADDITION TO SENTINEL-4 EEG
- K863193 — SENTINEL 4 EEG ANALYZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.