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FDA 510(k)

RICOH MEG

K-Number: K210199 · 2021-07-02

ApplicantRicoh Company, Ltd.
Decision Date2021-07-02
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RICOH MEG is a medical device manufactured by Ricoh Company, Ltd.. It received FDA 510(k) clearance on 2021-07-02 under approval number K210199. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICOH MEG?

RICOH MEG is a medical device that received FDA 510(k) clearance on 2021-07-02. It is manufactured by Ricoh Company, Ltd.. The 510(k) number is K210199.

When was RICOH MEG approved by the FDA?

RICOH MEG received FDA 510(k) clearance on 2021-07-02, under approval number K210199.

What company makes RICOH MEG?

RICOH MEG is manufactured by Ricoh Company, Ltd..

What is the FDA product code for RICOH MEG?

The FDA product code for RICOH MEG is OLX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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