FDA 510(k)

MINIMA S 系統

K 號：K231925 · 2023-07-11

決定日期2023-07-11

產品代碼LZO

諮詢委員會或

決定相當於

器材摘要

MINIMA S System is the device name listed in this FDA 510(k) record. The listed applicant is Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2023-07-11 under 510(k) number K231925. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MINIMA S System?

MINIMA S System is a medical device that received FDA 510(k) clearance on 2023-07-11. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K231925.

When did MINIMA S System receive FDA 510(k) clearance?

MINIMA S System received FDA 510(k) clearance on 2023-07-11, under 510(k) number K231925.

Who is the listed applicant for MINIMA S System?

The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINIMA S System?

The FDA product code for MINIMA S System is LZO.

其他以 Lima Corporate S.P.A. 為申請人之記錄

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相關器械（代碼：LZO）

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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