Rextar Pro
K号: K242185 · 2024-12-04
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决定日期2024-12-04
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
Rextar Pro is the device name listed in this FDA 510(k) record. The listed applicant is Raypia Co., Ltd.. It received FDA 510(k) clearance on 2024-12-04 under 510(k) number K242185. 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 Rextar Pro?
Rextar Pro is a medical device that received FDA 510(k) clearance on 2024-12-04. The listed applicant is Raypia Co., Ltd.. The 510(k) number is K242185.
When did Rextar Pro receive FDA 510(k) clearance?
Rextar Pro received FDA 510(k) clearance on 2024-12-04, under 510(k) number K242185.
Who is the listed applicant for Rextar Pro?
The FDA 510(k) record lists Raypia Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Rextar Pro?
The FDA product code for Rextar Pro is EHD.
相关临床试验
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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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