KERATOPLASTY SUTURING LENS— 510(k) K940106

Name: FDA 510(k) clearance K940106
Creator: U.S. Food and Drug Administration
Published: 1994-05-25

Substantially Equivalent

Visionary Technologies of Miami, Inc.

FDA 510(k) clearance K940106 for KERATOPLASTY SUTURING LENS, Substantially Equivalent on 1994-05-25. Applicant: Visionary Technologies of Miami, Inc.. Device class: Unclassified.

Clearance details

Applicant: Visionary Technologies of Miami, Inc.
Product code: Code HPX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1994-01-10
Decision date: 1994-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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