Axon Systems, Inc.
FDA 510(k) medical device clearances.
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.