AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201— 510(k) K983072

Substantially Equivalent

Nihon Kohden America, Inc.

FDA 510(k) clearance K983072 for AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201, Substantially Equivalent on 1998-12-01. Applicant: Nihon Kohden America, Inc..

Clearance details

Applicant: Nihon Kohden America, Inc.
Product code: Code OLV
Advisory panel: Neurology
Date received: 1998-09-02
Decision date: 1998-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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