FDA 510(k)

CT/MR 兼容 M.A.C. 陰道間質模板

K 號：K150979 · 2016-05-31

決定日期2016-05-31

產品代碼JAQ

諮詢委員會RA

決定相當於

器材摘要

CT/MR Compatible M.A.C. Interstitial GYN Template is the device name listed in this FDA 510(k) record. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 2016-05-31 under 510(k) number K150979. 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 CT/MR Compatible M.A.C. Interstitial GYN Template?

CT/MR Compatible M.A.C. Interstitial GYN Template is a medical device that received FDA 510(k) clearance on 2016-05-31. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K150979.

When did CT/MR Compatible M.A.C. Interstitial GYN Template receive FDA 510(k) clearance?

CT/MR Compatible M.A.C. Interstitial GYN Template received FDA 510(k) clearance on 2016-05-31, under 510(k) number K150979.

Who is the listed applicant for CT/MR Compatible M.A.C. Interstitial GYN Template?

The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CT/MR Compatible M.A.C. Interstitial GYN Template?

The FDA product code for CT/MR Compatible M.A.C. Interstitial GYN Template is JAQ.

其他以 Mick Radio-Nuclear Instruments, 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。

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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。

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官方來源

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