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FDA 510(k)

ParaMotion

K 號：K203761 · 2022-01-21

申請人Powerbasetec GmbH
決定日期2022-01-21
產品代碼IPL
諮詢委員會PM
決定相當於

器材摘要

ParaMotion is the device name listed in this FDA 510(k) record. The listed applicant is Powerbasetec GmbH. It received FDA 510(k) clearance on 2022-01-21 under 510(k) number K203761. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ParaMotion?

ParaMotion is a medical device that received FDA 510(k) clearance on 2022-01-21. The listed applicant is Powerbasetec GmbH. The 510(k) number is K203761.

When did ParaMotion receive FDA 510(k) clearance?

ParaMotion received FDA 510(k) clearance on 2022-01-21, under 510(k) number K203761.

Who is the listed applicant for ParaMotion?

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

What is the FDA product code for ParaMotion?

The FDA product code for ParaMotion is IPL.

相關臨床試驗

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相關器械（代碼：IPL）

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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