COMPUTERIZED ELECTRO-OCULOGRAPH— 510(k) K790637

Name: FDA 510(k) clearance K790637
Creator: U.S. Food and Drug Administration
Published: 1979-08-28

Substantially Equivalent

Potomac Medical System

FDA 510(k) clearance K790637 for COMPUTERIZED ELECTRO-OCULOGRAPH, Substantially Equivalent on 1979-08-28. Applicant: Potomac Medical System. Device class: 2.

Clearance details

Applicant: Potomac Medical System
Product code: Code HLX
Device class: Class 2
Regulation: 21 CFR 886.1630
Advisory panel: Ophthalmic
Date received: 1979-04-02
Decision date: 1979-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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