自动折叠轮椅，S21F
K号: K220227 · 2022-10-12
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决定日期2022-10-12
产品代码INI
咨询委员会PM
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决定实质等同
器械摘要
Auto Folding Scooter, S21F is the device name listed in this FDA 510(k) record. The listed applicant is Heartway Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2022-10-12 under 510(k) number K220227. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Auto Folding Scooter, S21F?
Auto Folding Scooter, S21F is a medical device that received FDA 510(k) clearance on 2022-10-12. The listed applicant is Heartway Medical Products Co., Ltd.. The 510(k) number is K220227.
When did Auto Folding Scooter, S21F receive FDA 510(k) clearance?
Auto Folding Scooter, S21F received FDA 510(k) clearance on 2022-10-12, under 510(k) number K220227.
Who is the listed applicant for Auto Folding Scooter, S21F?
The FDA 510(k) record lists Heartway Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Auto Folding Scooter, S21F?
The FDA product code for Auto Folding Scooter, S21F is INI.
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。
相关器械（代码：INI）
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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