EDI VERIS SYSTEM— 510(k) K983983

Substantially Equivalent

Electro-Diagnostic Imaging, Inc.

FDA 510(k) clearance K983983 for EDI VERIS SYSTEM, Substantially Equivalent on 1999-02-03. Applicant: Electro-Diagnostic Imaging, Inc..

Clearance details

Applicant: Electro-Diagnostic Imaging, Inc.
Product code: Code HLX
Advisory panel: Ophthalmic
Date received: 1998-11-09
Decision date: 1999-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Altos, CA, US

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