CORNEAL ANALYSIS SYSTEMS(TM)— 510(k) K924032

Name: FDA 510(k) clearance K924032
Creator: U.S. Food and Drug Administration
Published: 1993-03-18

Substantially Equivalent

Eyesys Laboratories, Inc.

FDA 510(k) clearance K924032 for CORNEAL ANALYSIS SYSTEMS(TM), Substantially Equivalent on 1993-03-18. Applicant: Eyesys Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Eyesys Laboratories, Inc.
Product code: Code HQY
Device class: Class 1
Regulation: 21 CFR 886.5850
Advisory panel: Ophthalmic
Date received: 1992-08-11
Decision date: 1993-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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