PHOENIX DIGITAL EEG— 510(k) K002316

Substantially Equivalent

Axon Systems, Inc.

FDA 510(k) clearance K002316 for PHOENIX DIGITAL EEG, Substantially Equivalent on 2000-10-26. Applicant: Axon Systems, Inc..

Clearance details

Applicant: Axon Systems, Inc.
Product code: Code GWQ
Advisory panel: Neurology
Date received: 2000-07-31
Decision date: 2000-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.