重叠压缩治疗
K号: K202839 · 2021-01-21
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器械摘要
常见问题
What is the Overlapped Compression Therapy?
Overlapped Compression Therapy is a medical device that received FDA 510(k) clearance on 2021-01-21. The listed applicant is Jkh Health Co., Ltd.. The 510(k) number is K202839.
When did Overlapped Compression Therapy receive FDA 510(k) clearance?
Overlapped Compression Therapy received FDA 510(k) clearance on 2021-01-21, under 510(k) number K202839.
Who is the listed applicant for Overlapped Compression Therapy?
The FDA 510(k) record lists Jkh Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Overlapped Compression Therapy?
The FDA product code for Overlapped Compression Therapy is JOW.
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Jkh Health Co., Ltd.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:JOW)
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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