FDA 510(k)

FBC 921 (ALIF)

K 號：K180695 · 2018-07-12

決定日期2018-07-12

產品代碼OVD

諮詢委員會或

決定相當於

器材摘要

FBC 921 (ALIF) is the device name listed in this FDA 510(k) record. The listed applicant is Fbc Device Aps. It received FDA 510(k) clearance on 2018-07-12 under 510(k) number K180695. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the FBC 921 (ALIF)?

FBC 921 (ALIF) is a medical device that received FDA 510(k) clearance on 2018-07-12. The listed applicant is Fbc Device Aps. The 510(k) number is K180695.

When did FBC 921 (ALIF) receive FDA 510(k) clearance?

FBC 921 (ALIF) received FDA 510(k) clearance on 2018-07-12, under 510(k) number K180695.

Who is the listed applicant for FBC 921 (ALIF)?

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

What is the FDA product code for FBC 921 (ALIF)?

The FDA product code for FBC 921 (ALIF) is OVD.

相關器械（代碼：OVD）

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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