IsoSphere
K 號：K242818 · 2025-07-15
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器材摘要
IsoSphere is the device name listed in this FDA 510(k) record. The listed applicant is Isoaid, LLC. It received FDA 510(k) clearance on 2025-07-15 under 510(k) number K242818. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the IsoSphere?
IsoSphere is a medical device that received FDA 510(k) clearance on 2025-07-15. The listed applicant is Isoaid, LLC. The 510(k) number is K242818.
When did IsoSphere receive FDA 510(k) clearance?
IsoSphere received FDA 510(k) clearance on 2025-07-15, under 510(k) number K242818.
Who is the listed applicant for IsoSphere?
The FDA 510(k) record lists Isoaid, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IsoSphere?
The FDA product code for IsoSphere is KXK.
相關臨床試驗
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相關器械（代碼：KXK）
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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