FDA 510(k)

AOS 标记种子 (SMG0242-025)

K 號：K233626 · 2024-07-02

決定日期2024-07-02

產品代碼JAQ

諮詢委員會RA

決定相當於

器材摘要

AOS Marker Seeds (SMG0242-025) is the device name listed in this FDA 510(k) record. The listed applicant is Alpha-Omega Services, Inc.. It received FDA 510(k) clearance on 2024-07-02 under 510(k) number K233626. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AOS Marker Seeds (SMG0242-025)?

AOS Marker Seeds (SMG0242-025) is a medical device that received FDA 510(k) clearance on 2024-07-02. The listed applicant is Alpha-Omega Services, Inc.. The 510(k) number is K233626.

When did AOS Marker Seeds (SMG0242-025) receive FDA 510(k) clearance?

AOS Marker Seeds (SMG0242-025) received FDA 510(k) clearance on 2024-07-02, under 510(k) number K233626.

Who is the listed applicant for AOS Marker Seeds (SMG0242-025)?

The FDA 510(k) record lists Alpha-Omega Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AOS Marker Seeds (SMG0242-025)?

The FDA product code for AOS Marker Seeds (SMG0242-025) is JAQ.

其他以 Alpha-Omega Services, Inc. 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。

K233628AOS 間隙模板、針和附件

相關器械（代碼：JAQ）

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。

K262383LumenCare 銀河Nucletron B.V.K252717MAASTRO 直腸施藥器組Varian Medical Systems K251037直腸施藥器Nucletron B.V.K252884導向阿魯斯應用器組Varian Medical Systems K250299CT/ MR 串聯及卵形組合Varian Medical Systems, Inc.K250289內腔/間質系統Varian Medical Systems

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。