FDA 510(k)

結縫設備

K 號：K172985 · 2018-06-14

決定日期2018-06-14

產品代碼FHN

諮詢委員會GU

決定相當於

器材摘要

Ligation Device is the device name listed in this FDA 510(k) record. The listed applicant is Leo Medical Co., Ltd.. It received FDA 510(k) clearance on 2018-06-14 under 510(k) number K172985. The device is classified under product code FHN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ligation Device?

Ligation Device is a medical device that received FDA 510(k) clearance on 2018-06-14. The listed applicant is Leo Medical Co., Ltd.. The 510(k) number is K172985.

When did Ligation Device receive FDA 510(k) clearance?

Ligation Device received FDA 510(k) clearance on 2018-06-14, under 510(k) number K172985.

Who is the listed applicant for Ligation Device?

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

What is the FDA product code for Ligation Device?

The FDA product code for Ligation Device is FHN.

其他以 Leo Medical Co., Ltd. 為申請人之記錄

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相關器械（代碼：FHN）

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。

K213223多波段縫合器Beijing Zksk Technology Co., Ltd.

官方來源

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