FDA 510(k)

飛利浦 VSC-MEDlib

K 號：K242001 · 2025-04-04

申請人Philips Medical Systems Nederland B.V.

決定日期2025-04-04

產品代碼BZQ

諮詢委員會AN

決定相當於

器材摘要

Philips VSC-MEDlib is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2025-04-04 under 510(k) number K242001. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Philips VSC-MEDlib?

Philips VSC-MEDlib is a medical device that received FDA 510(k) clearance on 2025-04-04. The listed applicant is Philips Medical Systems Nederland B.V.. The 510(k) number is K242001.

When did Philips VSC-MEDlib receive FDA 510(k) clearance?

Philips VSC-MEDlib received FDA 510(k) clearance on 2025-04-04, under 510(k) number K242001.

Who is the listed applicant for Philips VSC-MEDlib?

FDA 510(k) 記錄將 Philips Medical Systems Nederland B.V. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Philips VSC-MEDlib?

The FDA product code for Philips VSC-MEDlib is BZQ.

其他以 Philips Medical Systems Nederland B.V. 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。

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相關器械（代碼：BZQ）

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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