RiX70 DC
K号: K182206 · 2018-09-13
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决定日期2018-09-13
产品代码EHD
咨询委员会DE
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决定实质等同
器械摘要
RiX70 DC is the device name listed in this FDA 510(k) record. The listed applicant is Trident S.R.L. It received FDA 510(k) clearance on 2018-09-13 under 510(k) number K182206. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the RiX70 DC?
RiX70 DC is a medical device that received FDA 510(k) clearance on 2018-09-13. The listed applicant is Trident S.R.L. The 510(k) number is K182206.
When did RiX70 DC receive FDA 510(k) clearance?
RiX70 DC received FDA 510(k) clearance on 2018-09-13, under 510(k) number K182206.
Who is the listed applicant for RiX70 DC?
The FDA 510(k) record lists Trident S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RiX70 DC?
The FDA product code for RiX70 DC is EHD.
列明Trident S.R.L为申报人的其他记录
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。
相关器械（代码：EHD）
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。
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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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