威利手动轮椅
K号: K152827 · 2016-02-19
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申请人Rupiani
决定日期2016-02-19
产品代码IOR
咨询委员会PM
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决定实质等同
器械摘要
Weely Manual Wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Rupiani. It received FDA 510(k) clearance on 2016-02-19 under 510(k) number K152827. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Weely Manual Wheelchair?
Weely Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2016-02-19. The listed applicant is Rupiani. The 510(k) number is K152827.
When did Weely Manual Wheelchair receive FDA 510(k) clearance?
Weely Manual Wheelchair received FDA 510(k) clearance on 2016-02-19, under 510(k) number K152827.
Who is the listed applicant for Weely Manual Wheelchair?
The FDA 510(k) record lists Rupiani as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Weely Manual Wheelchair?
The FDA product code for Weely Manual Wheelchair is IOR.
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：IOR）
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
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