GELENDER VACUUM FIXATION RING SYS— 510(k) K832912

Name: FDA 510(k) clearance K832912
Creator: U.S. Food and Drug Administration
Published: 1984-01-10

Substantially Equivalent

Miami Eye Technology, Inc.

FDA 510(k) clearance K832912 for GELENDER VACUUM FIXATION RING SYS, Substantially Equivalent on 1984-01-10. Applicant: Miami Eye Technology, Inc.. Device class: 1.

Clearance details

Applicant: Miami Eye Technology, Inc.
Product code: Code HNH
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1983-08-29
Decision date: 1984-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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