Air Relax，可压缩肢体袖套系统（型号：AR-1.0，AR-2.0）
K号: K191441 · 2021-03-05
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器械摘要
常见问题
What is the Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0)?
Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0) is a medical device that received FDA 510(k) clearance on 2021-03-05. The listed applicant is Maxstar Industrial Co., Ltd.. The 510(k) number is K191441.
When did Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0) receive FDA 510(k) clearance?
Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0) received FDA 510(k) clearance on 2021-03-05, under 510(k) number K191441.
Who is the listed applicant for Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0)?
The FDA 510(k) record lists Maxstar Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0)?
The FDA product code for Air Relax, Compressible Limb Sleeve System (Model: AR-1.0, AR-2.0) is IRP.
相关临床试验
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列明Maxstar Industrial 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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