Saans (F4-01-00-000-000)
K 號：K251165 · 2026-01-06
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器材摘要
Saans (F4-01-00-000-000) is the device name listed in this FDA 510(k) record. The listed applicant is Innaccel Technologies Private Limited. It received FDA 510(k) clearance on 2026-01-06 under 510(k) number K251165. The device is classified under product code SGR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Saans (F4-01-00-000-000)?
Saans (F4-01-00-000-000) is a medical device that received FDA 510(k) clearance on 2026-01-06. The listed applicant is Innaccel Technologies Private Limited. The 510(k) number is K251165.
When did Saans (F4-01-00-000-000) receive FDA 510(k) clearance?
Saans (F4-01-00-000-000) received FDA 510(k) clearance on 2026-01-06, under 510(k) number K251165.
Who is the listed applicant for Saans (F4-01-00-000-000)?
The FDA 510(k) record lists Innaccel Technologies Private Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Saans (F4-01-00-000-000)?
The FDA product code for Saans (F4-01-00-000-000) is SGR.
相關臨床試驗
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相關器械（代碼：SGR）
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。
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