FDA 510(k)

終端蓋

K 號：K210461 · 2021-09-14

決定日期2021-09-14

產品代碼MSD

諮詢委員會GU

決定相當於

器材摘要

End Cap is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components Inc (Medcomp). It received FDA 510(k) clearance on 2021-09-14 under 510(k) number K210461. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the End Cap?

End Cap is a medical device that received FDA 510(k) clearance on 2021-09-14. The listed applicant is Medical Components Inc (Medcomp). The 510(k) number is K210461.

When did End Cap receive FDA 510(k) clearance?

End Cap received FDA 510(k) clearance on 2021-09-14, under 510(k) number K210461.

Who is the listed applicant for End Cap?

The FDA 510(k) record lists Medical Components Inc (Medcomp) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for End Cap?

The FDA product code for End Cap is MSD.

相關器械（代碼：MSD）

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。

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官方來源

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