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FDA 510(k)

Tua Face Fitness / Tua Trend Face 医療設備規範文本 Tua Face Fitness / Tua Trend Face 医療設備之規範性文件 Tua Face Fitness / Tua Trend Face 製品之醫療設備規範 Tua Face Fitness / Tua Trend Face 醫療設備之FDA許可、510(k)認證、PMA認證、NCT、PMID、識別碼及網址 規範政策:medical-regulatory-v1

K 號:K192077 · 2020-09-30

決定日期2020-09-30
產品代碼NFO
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

Tua Face Fitness / Tua Trend Face is the device name listed in this FDA 510(k) record. The listed applicant is Vupiesse S.R.L. It received FDA 510(k) clearance on 2020-09-30 under 510(k) number K192077. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tua Face Fitness / Tua Trend Face?

Tua Face Fitness / Tua Trend Face is a medical device that received FDA 510(k) clearance on 2020-09-30. The listed applicant is Vupiesse S.R.L. The 510(k) number is K192077.

When did Tua Face Fitness / Tua Trend Face receive FDA 510(k) clearance?

Tua Face Fitness / Tua Trend Face received FDA 510(k) clearance on 2020-09-30, under 510(k) number K192077.

Who is the listed applicant for Tua Face Fitness / Tua Trend Face?

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

What is the FDA product code for Tua Face Fitness / Tua Trend Face?

The FDA product code for Tua Face Fitness / Tua Trend Face is NFO.

相關臨床試驗

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相關器械(代碼:NFO)

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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