RICOH MEG— 510(k) K210199

Substantially Equivalent

Ricoh Company, Ltd.

FDA 510(k) clearance K210199 for RICOH MEG, Substantially Equivalent on 2021-07-02. Applicant: Ricoh Company, Ltd.. Device class: 2.

Clearance details

Applicant: Ricoh Company, Ltd.
Product code: Code OLX
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2021-01-25
Decision date: 2021-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kanazawa-Shi, JP

Download summary PDF View on FDA.gov ↗

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