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FDA 510(k)

Uro-G 腹腔鏡

K 號:K202921 · 2021-05-04

決定日期2021-05-04
產品代碼FAJ
諮詢委員會GU
決定相當於

器材摘要

Uro-G Cystoscope is the device name listed in this FDA 510(k) record. The listed applicant is Uroviu Corporation. It received FDA 510(k) clearance on 2021-05-04 under 510(k) number K202921. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Uro-G Cystoscope?

Uro-G Cystoscope is a medical device that received FDA 510(k) clearance on 2021-05-04. The listed applicant is Uroviu Corporation. The 510(k) number is K202921.

When did Uro-G Cystoscope receive FDA 510(k) clearance?

Uro-G Cystoscope received FDA 510(k) clearance on 2021-05-04, under 510(k) number K202921.

Who is the listed applicant for Uro-G Cystoscope?

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

What is the FDA product code for Uro-G Cystoscope?

The FDA product code for Uro-G Cystoscope is FAJ.

相關臨床試驗

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其他以 Uroviu Corporation 為申請人之記錄

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相關器械(代碼:FAJ)

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官方來源

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