FDA 510(k)

XVbeam2000

K 號：K233914 · 2024-02-08

申請人Shenzhen Xpectvision Technology Co., Ltd.

決定日期2024-02-08

產品代碼EHD

諮詢委員會DE

決定相當於

器材摘要

XVbeam2000 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Xpectvision Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-02-08 under 510(k) number K233914. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the XVbeam2000?

XVbeam2000 is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is Shenzhen Xpectvision Technology Co., Ltd.. The 510(k) number is K233914.

When did XVbeam2000 receive FDA 510(k) clearance?

XVbeam2000 received FDA 510(k) clearance on 2024-02-08, under 510(k) number K233914.

Who is the listed applicant for XVbeam2000?

The FDA 510(k) record lists Shenzhen Xpectvision Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XVbeam2000?

The FDA product code for XVbeam2000 is EHD.

其他以 Shenzhen Xpectvision Technology Co., Ltd. 為申請人之記錄

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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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