FDA 510(k)

Ezlymph, Ezlymph M

K 號：K193662 · 2021-02-11

決定日期2021-02-11

產品代碼JOW

諮詢委員會履歷

決定相當於

器材摘要

Ezlymph, Ezlymph M is the device name listed in this FDA 510(k) record. The listed applicant is Eezcare Medical Corp. It received FDA 510(k) clearance on 2021-02-11 under 510(k) number K193662. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ezlymph, Ezlymph M?

Ezlymph, Ezlymph M is a medical device that received FDA 510(k) clearance on 2021-02-11. The listed applicant is Eezcare Medical Corp. The 510(k) number is K193662.

When did Ezlymph, Ezlymph M receive FDA 510(k) clearance?

Ezlymph, Ezlymph M received FDA 510(k) clearance on 2021-02-11, under 510(k) number K193662.

Who is the listed applicant for Ezlymph, Ezlymph M?

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

What is the FDA product code for Ezlymph, Ezlymph M?

The FDA product code for Ezlymph, Ezlymph M is JOW.

其他以 Eezcare Medical Corp 為申請人之記錄

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相關器械（代碼：JOW）

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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