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FDA 510(k)

31P/1H 頭线圈,23Na/1H 頭线圈,13C/1H 頭线圈

K 號:K213480 · 2023-02-01

決定日期2023-02-01
產品代碼MOS
諮詢委員會RA
決定相當於

器材摘要

31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil is the device name listed in this FDA 510(k) record. The listed applicant is Rapid Biomedical GmbH. It received FDA 510(k) clearance on 2023-02-01 under 510(k) number K213480. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil?

31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil is a medical device that received FDA 510(k) clearance on 2023-02-01. The listed applicant is Rapid Biomedical GmbH. The 510(k) number is K213480.

When did 31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil receive FDA 510(k) clearance?

31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil received FDA 510(k) clearance on 2023-02-01, under 510(k) number K213480.

Who is the listed applicant for 31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil?

The FDA 510(k) record lists Rapid Biomedical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil?

The FDA product code for 31P/1H Head Coil, 23Na/1H Head Coil, 13C/1H Head Coil is MOS.

其他以 Rapid Biomedical GmbH 為申請人之記錄

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相關器械(代碼:MOS)

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。

官方來源

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