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FDA 510(k)

飛利浦 IntelliVue 監護軟體

K 號:K161767 · 2017-01-27

決定日期2017-01-27
產品代碼DXJ
諮詢委員會履歷
決定相當於

器材摘要

Philips IntelliVue GuardianSoftware is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. It received FDA 510(k) clearance on 2017-01-27 under 510(k) number K161767. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Philips IntelliVue GuardianSoftware?

Philips IntelliVue GuardianSoftware is a medical device that received FDA 510(k) clearance on 2017-01-27. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K161767.

When did Philips IntelliVue GuardianSoftware receive FDA 510(k) clearance?

Philips IntelliVue GuardianSoftware received FDA 510(k) clearance on 2017-01-27, under 510(k) number K161767.

Who is the listed applicant for Philips IntelliVue GuardianSoftware?

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

What is the FDA product code for Philips IntelliVue GuardianSoftware?

The FDA product code for Philips IntelliVue GuardianSoftware is DXJ.

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其他以 Philips Medizin Systeme Boeblingen GmbH 為申請人之記錄

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相關器械(代碼:DXJ)

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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