FDA 510(k)

萊克塞爾伽馬計劃

K 號：K173791 · 2018-02-09

決定日期2018-02-09

產品代碼IWB

諮詢委員會RA

決定相當於

器材摘要

Leksell GammaPlan is the device name listed in this FDA 510(k) record. The listed applicant is Elekta Instrument AB. It received FDA 510(k) clearance on 2018-02-09 under 510(k) number K173791. The device is classified under product code IWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Leksell GammaPlan?

Leksell GammaPlan is a medical device that received FDA 510(k) clearance on 2018-02-09. The listed applicant is Elekta Instrument AB. The 510(k) number is K173791.

When did Leksell GammaPlan receive FDA 510(k) clearance?

Leksell GammaPlan received FDA 510(k) clearance on 2018-02-09, under 510(k) number K173791.

Who is the listed applicant for Leksell GammaPlan?

The FDA 510(k) record lists Elekta Instrument AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Leksell GammaPlan?

The FDA product code for Leksell GammaPlan is IWB.

其他以 Elekta Instrument AB 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。

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相關器械（代碼：IWB）

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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