Reaxon Plus— 510(k) K180222

Substantially Equivalent

Medovent GmbH

FDA 510(k) clearance K180222 for Reaxon Plus, Substantially Equivalent on 2018-04-24. Applicant: Medovent GmbH. Device class: 2.

Clearance details

Applicant: Medovent GmbH
Product code: Code JXI
Device class: Class 2
Regulation: 21 CFR 882.5275
Advisory panel: Neurology
Date received: 2018-01-25
Decision date: 2018-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mainz, DE

Download summary PDF View on FDA.gov ↗

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More clearances from Medovent GmbH

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