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FDA 510(k)

括約肌斷刀 / 短線兼容型,无菌括約肌斷刀

K 號:K210934 · 2021-12-01

決定日期2021-12-01
產品代碼KNS
諮詢委員會GU
決定相當於

器材摘要

Sphincterotome / short-wire compatible, Sterile Sphincterotome is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2021-12-01 under 510(k) number K210934. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sphincterotome / short-wire compatible, Sterile Sphincterotome?

Sphincterotome / short-wire compatible, Sterile Sphincterotome is a medical device that received FDA 510(k) clearance on 2021-12-01. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K210934.

When did Sphincterotome / short-wire compatible, Sterile Sphincterotome receive FDA 510(k) clearance?

Sphincterotome / short-wire compatible, Sterile Sphincterotome received FDA 510(k) clearance on 2021-12-01, under 510(k) number K210934.

Who is the listed applicant for Sphincterotome / short-wire compatible, Sterile Sphincterotome?

The FDA 510(k) record lists Micro-Tech (Nanjing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sphincterotome / short-wire compatible, Sterile Sphincterotome?

The FDA product code for Sphincterotome / short-wire compatible, Sterile Sphincterotome is KNS.

相關臨床試驗

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其他以 Micro-Tech (Nanjing) Co., Ltd. 為申請人之記錄

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相關器械(代碼:KNS)

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

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