NEURODYN RUBY MUSCLE STIMULATOR, NEURODYN AUSSIE MUSCLE STIMULATOR— 510(k) K121369

Name: FDA 510(k) clearance K121369
Creator: U.S. Food and Drug Administration
Published: 2012-12-19

Substantially Equivalent

Ibramed Equipamentos Medicos

FDA 510(k) clearance K121369 for NEURODYN RUBY MUSCLE STIMULATOR, NEURODYN AUSSIE MUSCLE STIMULATOR, Substantially Equivalent on 2012-12-19. Applicant: Ibramed Equipamentos Medicos. Device class: 2.

Clearance details

Applicant: Ibramed Equipamentos Medicos
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2012-05-07
Decision date: 2012-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aventura, FL, 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.