免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

Swoop 開放式床邊磁共振斷層掃描系統

K 號:K212456 · 2021-11-17

決定日期2021-11-17
產品代碼LNH
諮詢委員會RA
決定相當於

器材摘要

Swoop 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, Inc.. It received FDA 510(k) clearance on 2021-11-17 under 510(k) number K212456. 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 Swoop Point-of-Care Magnetic Resonance Imaging (POC MRI) Scanner System?

Swoop Point-of-Care Magnetic Resonance Imaging (POC MRI) Scanner System is a medical device that received FDA 510(k) clearance on 2021-11-17. The listed applicant is Hyperfine, Inc.. The 510(k) number is K212456.

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

Swoop Point-of-Care Magnetic Resonance Imaging (POC MRI) Scanner System received FDA 510(k) clearance on 2021-11-17, under 510(k) number K212456.

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

FDA 510(k) 記錄將 Hyperfine, Inc. 列為申請人。這並不單獨確立設備製造商。

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

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

相關臨床試驗

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。

其他以 Hyperfine, 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。

查看所有 14 項裝置 →

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

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。

↑