MEC-I-TRON MINI, MODEL M-2— 510(k) K895289

Name: FDA 510(k) clearance K895289
Creator: U.S. Food and Drug Administration
Published: 1990-01-19

Substantially Equivalent

Meyer Equipment Company, Inc.

FDA 510(k) clearance K895289 for MEC-I-TRON MINI, MODEL M-2, Substantially Equivalent on 1990-01-19. Applicant: Meyer Equipment Company, Inc.. Device class: 2.

Clearance details

Applicant: Meyer Equipment Company, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1989-08-25
Decision date: 1990-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lee'S Summit, MO, US

Download summary PDF View on FDA.gov ↗

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