MTI PHOTOSCREENER— 510(k) K934880

Name: FDA 510(k) clearance K934880
Creator: U.S. Food and Drug Administration
Published: 1994-04-06

Substantially Equivalent

Medical Technology and Innovations, Inc.

FDA 510(k) clearance K934880 for MTI PHOTOSCREENER, Substantially Equivalent on 1994-04-06. Applicant: Medical Technology and Innovations, Inc.. Device class: 2.

Clearance details

Applicant: Medical Technology and Innovations, Inc.
Product code: Code MMF
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 1993-10-12
Decision date: 1994-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cedar Falls, IA, US

Download summary PDF View on FDA.gov ↗

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