Neurodyn V2.0, Neurodyn Aussie V2.0— 510(k) K210572

Name: FDA 510(k) clearance K210572
Creator: U.S. Food and Drug Administration
Published: 2021-05-11

Substantially Equivalent

Ibramed Equipamentos Medicos

FDA 510(k) clearance K210572 for Neurodyn V2.0, Neurodyn Aussie V2.0, Substantially Equivalent on 2021-05-11. Applicant: Ibramed Equipamentos Medicos. Device class: 2.

Clearance details

Applicant: Ibramed Equipamentos Medicos
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2021-02-26
Decision date: 2021-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amparo, BR

Download summary PDF View on FDA.gov ↗

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