AE-800PA EEG MODULE— 510(k) K884537

Substantially Equivalent

Nihon Kohden America, Inc.

FDA 510(k) clearance K884537 for AE-800PA EEG MODULE, Substantially Equivalent on 1988-12-29. Applicant: Nihon Kohden America, Inc..

Clearance details

Applicant: Nihon Kohden America, Inc.
Product code: Code GWQ
Advisory panel: Neurology
Date received: 1988-10-28
Decision date: 1988-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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