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FDA 510(k)

高精細即時醫療磁共振成像(POC MRI)掃描系統

K 號:K201722 · 2020-08-11

決定日期2020-08-11
產品代碼LNH
諮詢委員會RA
決定相當於

器材摘要

Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System is the device name listed in this FDA 510(k) record. The listed applicant is Hyperfine Research, Inc.. It received FDA 510(k) clearance on 2020-08-11 under 510(k) number K201722. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System?

Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System is a medical device that received FDA 510(k) clearance on 2020-08-11. The listed applicant is Hyperfine Research, Inc.. The 510(k) number is K201722.

When did Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System receive FDA 510(k) clearance?

Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System received FDA 510(k) clearance on 2020-08-11, under 510(k) number K201722.

Who is the listed applicant for Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System?

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

What is the FDA product code for Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System?

The FDA product code for Hyperfine Point-Of-Care Magnetic Resonance Imaging (POC MRI) Scanner System is LNH.

相關臨床試驗

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其他以 Hyperfine Research, 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。

相關器械(代碼:LNH)

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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