NEUROFAX 7310 SERIES (EEG)— 510(k) K854663

Substantially Equivalent

Nihon Kohden America, Inc.

FDA 510(k) clearance K854663 for NEUROFAX 7310 SERIES (EEG), Substantially Equivalent on 1986-08-20. Applicant: Nihon Kohden America, Inc..

Clearance details

Applicant: Nihon Kohden America, Inc.
Product code: Code GWQ
Advisory panel: Neurology
Date received: 1985-11-20
Decision date: 1986-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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