Contour 手腕/手（Q7000232）
K号: K233652 · 2024-02-16
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器械摘要
Contour Hand/Wrist (Q7000232) is the device name listed in this FDA 510(k) record. The listed applicant is Quality Electrodynamics. It received FDA 510(k) clearance on 2024-02-16 under 510(k) number K233652. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Contour Hand/Wrist (Q7000232)?
Contour Hand/Wrist (Q7000232) is a medical device that received FDA 510(k) clearance on 2024-02-16. The listed applicant is Quality Electrodynamics. The 510(k) number is K233652.
When did Contour Hand/Wrist (Q7000232) receive FDA 510(k) clearance?
Contour Hand/Wrist (Q7000232) received FDA 510(k) clearance on 2024-02-16, under 510(k) number K233652.
Who is the listed applicant for Contour Hand/Wrist (Q7000232)?
The FDA 510(k) record lists Quality Electrodynamics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Contour Hand/Wrist (Q7000232)?
The FDA product code for Contour Hand/Wrist (Q7000232) is MOS.
相关临床试验
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。
列明Quality Electrodynamics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：MOS）
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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