Sonomed IV, Sonomed V
K号: K202788 · 2021-12-23
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决定日期2021-12-23
产品代码IMI
咨询委员会PM
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决定实质等同
器械摘要
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.
常见问题
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.
相关临床试验
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相关器械（代码：IMI）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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