FDA 510(k)

BTL-899

K 號：K192224 · 2019-12-05

申請人Btl

決定日期2019-12-05

產品代碼GEI

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

BTL-899 is the device name listed in this FDA 510(k) record. The listed applicant is Btl. It received FDA 510(k) clearance on 2019-12-05 under 510(k) number K192224. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BTL-899?

BTL-899 is a medical device that received FDA 510(k) clearance on 2019-12-05. The listed applicant is Btl. The 510(k) number is K192224.

When did BTL-899 receive FDA 510(k) clearance?

BTL-899 received FDA 510(k) clearance on 2019-12-05, under 510(k) number K192224.

Who is the listed applicant for BTL-899?

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

What is the FDA product code for BTL-899?

The FDA product code for BTL-899 is GEI.

其他以 Btl 為申請人之記錄

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。

K202199BTL-899ST K200382BTL-703-2 K193201BTL-785F

相關器械（代碼：GEI）

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。

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官方來源

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