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FDA 510(k)

Tranberg CLS 激光施用器

K 號:K201466 · 2021-03-26

決定日期2021-03-26
產品代碼GEX
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

Tranberg CLS Laser Applicator is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Laserthermia Systems, AB. It received FDA 510(k) clearance on 2021-03-26 under 510(k) number K201466. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the Tranberg CLS Laser Applicator?

Tranberg CLS Laser Applicator is a medical device that received FDA 510(k) clearance on 2021-03-26. The listed applicant is Clinical Laserthermia Systems, AB. The 510(k) number is K201466.

When did Tranberg CLS Laser Applicator receive FDA 510(k) clearance?

Tranberg CLS Laser Applicator received FDA 510(k) clearance on 2021-03-26, under 510(k) number K201466.

Who is the listed applicant for Tranberg CLS Laser Applicator?

The FDA 510(k) record lists Clinical Laserthermia Systems, AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tranberg CLS Laser Applicator?

The FDA product code for Tranberg CLS Laser Applicator is GEX. This falls under the Gastroenterology category.

相關臨床試驗

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其他以 Clinical Laserthermia Systems, AB 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。

相關器械(代碼:GEX)

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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