PHOENIX DIGITAL EEG SYSTEM— 510(k) K911229

Substantially Equivalent

Dantec Medical, Inc.

FDA 510(k) clearance K911229 for PHOENIX DIGITAL EEG SYSTEM, Substantially Equivalent on 1991-09-30. Applicant: Dantec Medical, Inc..

Clearance details

Applicant: Dantec Medical, Inc.
Product code: Code GWQ
Advisory panel: Neurology
Date received: 1991-03-20
Decision date: 1991-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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