SURGICAL IOP MONITOR— 510(k) K832996

Name: FDA 510(k) clearance K832996
Creator: U.S. Food and Drug Administration
Published: 1983-11-28

Substantially Equivalent

Miami Eye Technology, Inc.

FDA 510(k) clearance K832996 for SURGICAL IOP MONITOR, Substantially Equivalent on 1983-11-28. Applicant: Miami Eye Technology, Inc.. Device class: 2.

Clearance details

Applicant: Miami Eye Technology, Inc.
Product code: Code HKY
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 1983-09-02
Decision date: 1983-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K831702 — RARE-EARTH INTRA-OCULAR MAGNET1983-06-30

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