Sonomed IV, Sonomed V
K 號：K202788 · 2021-12-23
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器材摘要
Sonomed IV, Sonomed V is the device name listed in this FDA 510(k) record. The listed applicant is Carci Industria E Comercio DE Aparelhos Cirurgicos E Orto. It received FDA 510(k) clearance on 2021-12-23 under 510(k) number K202788. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Sonomed IV, Sonomed V?
Sonomed IV, Sonomed V is a medical device that received FDA 510(k) clearance on 2021-12-23. The listed applicant is Carci Industria E Comercio DE Aparelhos Cirurgicos E Orto. The 510(k) number is K202788.
When did Sonomed IV, Sonomed V receive FDA 510(k) clearance?
Sonomed IV, Sonomed V received FDA 510(k) clearance on 2021-12-23, under 510(k) number K202788.
Who is the listed applicant for Sonomed IV, Sonomed V?
The FDA 510(k) record lists Carci Industria E Comercio DE Aparelhos Cirurgicos E Orto as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sonomed IV, Sonomed V?
The FDA product code for Sonomed IV, Sonomed V is IMI.
相關臨床試驗
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相關器械（代碼：IMI）
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
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