FDA 510(k)

預覽肩部

K 號：K240172 · 2024-04-04

決定日期2024-04-04

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

Preview Shoulder is the device name listed in this FDA 510(k) record. The listed applicant is Genesis Software Innovations. It received FDA 510(k) clearance on 2024-04-04 under 510(k) number K240172. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Preview Shoulder?

Preview Shoulder is a medical device that received FDA 510(k) clearance on 2024-04-04. The listed applicant is Genesis Software Innovations. The 510(k) number is K240172.

When did Preview Shoulder receive FDA 510(k) clearance?

Preview Shoulder received FDA 510(k) clearance on 2024-04-04, under 510(k) number K240172.

Who is the listed applicant for Preview Shoulder?

The FDA 510(k) record lists Genesis Software Innovations as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Preview Shoulder?

The FDA product code for Preview Shoulder is QIH.

其他以 Genesis Software Innovations 為申請人之記錄

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K210556預覽肩部

相關器械（代碼：QIH）

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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