FDA 510(k)

RICOH MEG

K-Number: K210199 · 2021-07-02

Decision Date2021-07-02

Product CodeOLX

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

RICOH MEG is the device name listed in this FDA 510(k) record. The listed applicant is Ricoh Company, Ltd.. It received FDA 510(k) clearance on 2021-07-02 under 510(k) 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. The listed applicant is Ricoh Company, Ltd.. The 510(k) number is K210199.

When did RICOH MEG receive FDA 510(k) clearance?

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

Who is the listed applicant for RICOH MEG?

The FDA 510(k) record lists Ricoh Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RICOH MEG?

The FDA product code for RICOH MEG is OLX.

Related Devices (Code: OLX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260563CN-Suite™FIND Surgical Sciences Inc. D/B/A FIND Neuro K252565PreOp v3Clouds of Care K250239NeuroMatchLVIS Corporation K241513SourcererBrain Electrophysiology Laboratory Company, LLC K233985TRIUX™ neo (NM27000N ); MEGreview (SW26241N-B)Megin OY K201910EZTrackNeurologic, LLC

Official Source

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