FDA 510(k)

NuEra Tight RF, NuEra Tight RF Plus

K 號：K210867 · 2021-04-21

決定日期2021-04-21

產品代碼PBX

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

NuEra Tight RF, NuEra Tight RF Plus is the device name listed in this FDA 510(k) record. The listed applicant is Bios S.R.L.. It received FDA 510(k) clearance on 2021-04-21 under 510(k) number K210867. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NuEra Tight RF, NuEra Tight RF Plus?

NuEra Tight RF, NuEra Tight RF Plus is a medical device that received FDA 510(k) clearance on 2021-04-21. The listed applicant is Bios S.R.L.. The 510(k) number is K210867.

When did NuEra Tight RF, NuEra Tight RF Plus receive FDA 510(k) clearance?

NuEra Tight RF, NuEra Tight RF Plus received FDA 510(k) clearance on 2021-04-21, under 510(k) number K210867.

Who is the listed applicant for NuEra Tight RF, NuEra Tight RF Plus?

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

What is the FDA product code for NuEra Tight RF, NuEra Tight RF Plus?

The FDA product code for NuEra Tight RF, NuEra Tight RF Plus is PBX.

其他以 Bios S.R.L. 為申請人之記錄

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相關器械（代碼：PBX）

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。

K243223多療法美容治療設備（BHS 202 UNYQUE）Bh Group Us, LLC K253480Capenergy C 裝置 RF C200 及 C400 DrakarianCapenergy Medical S.L.K260647規範化醫療設備名稱：SPECCHIOEl.En S.P.A.K253261Apollo Quattro (APQ-10M)Weero Co., Ltd.K252888NeoSculpt PlusS&M Medical Co., Ltd.K250734OptiLUV 裝置Pollogen, Ltd.

官方來源

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