VIRECTOMY LENS— 510(k) K940107

Name: FDA 510(k) clearance K940107
Creator: U.S. Food and Drug Administration
Published: 1994-09-06

Substantially Equivalent

Visionary Technologies of Miami, Inc.

FDA 510(k) clearance K940107 for VIRECTOMY LENS, Substantially Equivalent on 1994-09-06. Applicant: Visionary Technologies of Miami, Inc.. Device class: 2.

Clearance details

Applicant: Visionary Technologies of Miami, Inc.
Product code: Code HJK
Device class: Class 2
Regulation: 21 CFR 886.1385
Advisory panel: Ophthalmic
Date received: 1994-01-10
Decision date: 1994-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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K940106 — KERATOPLASTY SUTURING LENS1994-05-25

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