空气压缩治疗系统 FO-3001；空气压缩治疗系统 FO-3008
K号: K201982 · 2021-03-25
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器械摘要
常见问题
What is the Air compression therapy system FO-3001; Air compression therapy system FO-3008?
Air compression therapy system FO-3001; Air compression therapy system FO-3008 is a medical device that received FDA 510(k) clearance on 2021-03-25. The listed applicant is Foshan Hongfeng Co., Ltd.. The 510(k) number is K201982.
When did Air compression therapy system FO-3001; Air compression therapy system FO-3008 receive FDA 510(k) clearance?
Air compression therapy system FO-3001; Air compression therapy system FO-3008 received FDA 510(k) clearance on 2021-03-25, under 510(k) number K201982.
Who is the listed applicant for Air compression therapy system FO-3001; Air compression therapy system FO-3008?
The FDA 510(k) record lists Foshan Hongfeng Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air compression therapy system FO-3001; Air compression therapy system FO-3008?
The FDA product code for Air compression therapy system FO-3001; Air compression therapy system FO-3008 is IRP.
相关临床试验
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列明Foshan Hongfeng 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：IRP）
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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