LEE ALLEN'S UNIVERSAL MOTILITY IMPLANT— 510(k) K873578

Name: FDA 510(k) clearance K873578
Creator: U.S. Food and Drug Administration
Published: 1987-11-02

Substantially Equivalent

Oculo-Plastik Reg'D

FDA 510(k) clearance K873578 for LEE ALLEN'S UNIVERSAL MOTILITY IMPLANT, Substantially Equivalent on 1987-11-02. Applicant: Oculo-Plastik Reg'D. Device class: 2.

Clearance details

Applicant: Oculo-Plastik Reg'D
Product code: Code HPZ
Device class: Class 2
Regulation: 21 CFR 886.3320
Advisory panel: Ophthalmic
Date received: 1987-09-03
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada, CA

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Data sourced from openFDA. This site is unofficial and independent of the FDA.