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FDA 510(k)

I.T.S. PRS 鳳凰II

K 號:K260054 · 2026-04-24

申請人I.T.S. GmbH
決定日期2026-04-24
產品代碼HRS
諮詢委員會或
決定相當於

器材摘要

I.T.S. PRS Phoenix II is the device name listed in this FDA 510(k) record. The listed applicant is I.T.S. GmbH. It received FDA 510(k) clearance on 2026-04-24 under 510(k) number K260054. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the I.T.S. PRS Phoenix II?

I.T.S. PRS Phoenix II is a medical device that received FDA 510(k) clearance on 2026-04-24. The listed applicant is I.T.S. GmbH. The 510(k) number is K260054.

When did I.T.S. PRS Phoenix II receive FDA 510(k) clearance?

I.T.S. PRS Phoenix II received FDA 510(k) clearance on 2026-04-24, under 510(k) number K260054.

Who is the listed applicant for I.T.S. PRS Phoenix II?

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

What is the FDA product code for I.T.S. PRS Phoenix II?

The FDA product code for I.T.S. PRS Phoenix II is HRS.

相關臨床試驗

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其他以 I.T.S. GmbH 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:HRS)

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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