FDA 510(k)

骨抑制軟體

K 號：K240281 · 2024-05-31

決定日期2024-05-31

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

Bone Suppression Software is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta, Inc.. It received FDA 510(k) clearance on 2024-05-31 under 510(k) number K240281. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bone Suppression Software?

Bone Suppression Software is a medical device that received FDA 510(k) clearance on 2024-05-31. The listed applicant is Konica Minolta, Inc.. The 510(k) number is K240281.

When did Bone Suppression Software receive FDA 510(k) clearance?

Bone Suppression Software received FDA 510(k) clearance on 2024-05-31, under 510(k) number K240281.

Who is the listed applicant for Bone Suppression Software?

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

What is the FDA product code for Bone Suppression Software?

The FDA product code for Bone Suppression Software is LLZ.

其他以 Konica Minolta, Inc. 為申請人之記錄

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相關器械（代碼：LLZ）

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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