FDA 510(k)YY-A02-B 重叠压缩治疗
K号: K221862 · 2022-12-08
决定日期2022-12-08
产品代码IRP
咨询委员会PM
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决定实质等同
器械摘要
YY-A02-B Overlapped Compression Therapy is the device name listed in this FDA 510(k) record. The listed applicant is Huizhou Xinyi Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-12-08 under 510(k) number K221862. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the YY-A02-B Overlapped Compression Therapy?
YY-A02-B Overlapped Compression Therapy is a medical device that received FDA 510(k) clearance on 2022-12-08. The listed applicant is Huizhou Xinyi Technology Co., Ltd.. The 510(k) number is K221862.
When did YY-A02-B Overlapped Compression Therapy receive FDA 510(k) clearance?
YY-A02-B Overlapped Compression Therapy received FDA 510(k) clearance on 2022-12-08, under 510(k) number K221862.
Who is the listed applicant for YY-A02-B Overlapped Compression Therapy?
The FDA 510(k) record lists Huizhou Xinyi Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YY-A02-B Overlapped Compression Therapy?
The FDA product code for YY-A02-B Overlapped Compression Therapy is IRP.
相关临床试验
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列明Huizhou Xinyi Technology 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。
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