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FDA 510(k)

Tricoglam 家庭用

K 號:K193008 · 2020-12-03

決定日期2020-12-03
產品代碼OAP
諮詢委員會PM
決定相當於

器材摘要

Tricoglam Home Use is the device name listed in this FDA 510(k) record. The listed applicant is Advihair S.R.L.. It received FDA 510(k) clearance on 2020-12-03 under 510(k) number K193008. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tricoglam Home Use?

Tricoglam Home Use is a medical device that received FDA 510(k) clearance on 2020-12-03. The listed applicant is Advihair S.R.L.. The 510(k) number is K193008.

When did Tricoglam Home Use receive FDA 510(k) clearance?

Tricoglam Home Use received FDA 510(k) clearance on 2020-12-03, under 510(k) number K193008.

Who is the listed applicant for Tricoglam Home Use?

The FDA 510(k) record lists Advihair S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tricoglam Home Use?

The FDA product code for Tricoglam Home Use is OAP.

相關臨床試驗

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。

相關器械(代碼:OAP)

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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