FDA 510(k)

路徑 BGC

K 號：K260938 · 2026-04-15

決定日期2026-04-15

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

PATH BGC is the device name listed in this FDA 510(k) record. The listed applicant is Crossroads Neurovascular, Inc.. It received FDA 510(k) clearance on 2026-04-15 under 510(k) number K260938. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PATH BGC?

PATH BGC is a medical device that received FDA 510(k) clearance on 2026-04-15. The listed applicant is Crossroads Neurovascular, Inc.. The 510(k) number is K260938.

When did PATH BGC receive FDA 510(k) clearance?

PATH BGC received FDA 510(k) clearance on 2026-04-15, under 510(k) number K260938.

Who is the listed applicant for PATH BGC?

The FDA 510(k) record lists Crossroads Neurovascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATH BGC?

The FDA product code for PATH BGC is QJP.

其他以 Crossroads Neurovascular, Inc. 為申請人之記錄

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K242392路徑 BGC

相關器械（代碼：QJP）

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