DEKA PHYSIQ 360
K号: K231971 · 2023-09-26
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器械摘要
DEKA PHYSIQ 360 is the device name listed in this FDA 510(k) record. The listed applicant is El.En S.P.A.. It received FDA 510(k) clearance on 2023-09-26 under 510(k) number K231971. The device is classified under product code PKT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DEKA PHYSIQ 360?
DEKA PHYSIQ 360 is a medical device that received FDA 510(k) clearance on 2023-09-26. The listed applicant is El.En S.P.A.. The 510(k) number is K231971.
When did DEKA PHYSIQ 360 receive FDA 510(k) clearance?
DEKA PHYSIQ 360 received FDA 510(k) clearance on 2023-09-26, under 510(k) number K231971.
Who is the listed applicant for DEKA PHYSIQ 360?
The FDA 510(k) record lists El.En S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEKA PHYSIQ 360?
The FDA product code for DEKA PHYSIQ 360 is PKT.
相关临床试验
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列明El.En S.P.A.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：PKT）
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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