ds 頭部 32通道 3.0T
K 號：K213351 · 2021-10-29
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器材摘要
ds Head 32ch 3.0T is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation (Business Trade Name: Philips). It received FDA 510(k) clearance on 2021-10-29 under 510(k) number K213351. 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 ds Head 32ch 3.0T?
ds Head 32ch 3.0T is a medical device that received FDA 510(k) clearance on 2021-10-29. The listed applicant is Invivo Corporation (Business Trade Name: Philips). The 510(k) number is K213351.
When did ds Head 32ch 3.0T receive FDA 510(k) clearance?
ds Head 32ch 3.0T received FDA 510(k) clearance on 2021-10-29, under 510(k) number K213351.
Who is the listed applicant for ds Head 32ch 3.0T?
The FDA 510(k) record lists Invivo Corporation (Business Trade Name: Philips) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ds Head 32ch 3.0T?
The FDA product code for ds Head 32ch 3.0T is MOS.
其他以 Invivo Corporation (Business Trade Name: Philips) 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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