理光MEG
K 號：K210199 · 2021-07-02
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：OLX）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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