3.0T AIR 32CH HNA
K 號：K253738 · 2026-01-23
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器材摘要
3.0T AIR 32CH HNA is the device name listed in this FDA 510(k) record. The listed applicant is Ge Healthcare Coils (Usa Instruments, Inc.). It received FDA 510(k) clearance on 2026-01-23 under 510(k) number K253738. 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 3.0T AIR 32CH HNA?
3.0T AIR 32CH HNA is a medical device that received FDA 510(k) clearance on 2026-01-23. The listed applicant is Ge Healthcare Coils (Usa Instruments, Inc.). The 510(k) number is K253738.
When did 3.0T AIR 32CH HNA receive FDA 510(k) clearance?
3.0T AIR 32CH HNA received FDA 510(k) clearance on 2026-01-23, under 510(k) number K253738.
Who is the listed applicant for 3.0T AIR 32CH HNA?
The FDA 510(k) record lists Ge Healthcare Coils (Usa Instruments, Inc.) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3.0T AIR 32CH HNA?
The FDA product code for 3.0T AIR 32CH HNA is MOS.
其他以 Ge Healthcare Coils (Usa Instruments, Inc.) 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。
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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。
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