FDA 510(k)

MA012 铝制轮椅，MS019 钢制轮椅

K号: K231750 · 2023-08-15

申请人Sichuan Ast Medical Equipment Co., Ltd.

决定日期2023-08-15

产品代码IOR

咨询委员会PM 请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。

决定实质等同

器械摘要

MA012 Aluminum wheelchair, MS019 steel wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Sichuan Ast Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2023-08-15 under 510(k) number K231750. 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 MA012 Aluminum wheelchair, MS019 steel wheelchair?

MA012 Aluminum wheelchair, MS019 steel wheelchair is a medical device that received FDA 510(k) clearance on 2023-08-15. The listed applicant is Sichuan Ast Medical Equipment Co., Ltd.. The 510(k) number is K231750.

When did MA012 Aluminum wheelchair, MS019 steel wheelchair receive FDA 510(k) clearance?

MA012 Aluminum wheelchair, MS019 steel wheelchair received FDA 510(k) clearance on 2023-08-15, under 510(k) number K231750.

Who is the listed applicant for MA012 Aluminum wheelchair, MS019 steel wheelchair?

The FDA 510(k) record lists Sichuan Ast Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MA012 Aluminum wheelchair, MS019 steel wheelchair?

The FDA product code for MA012 Aluminum wheelchair, MS019 steel wheelchair is IOR.

列明Sichuan Ast Medical Equipment 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。

K242722手动轮椅（MASY23）K181795AST Model MA012和MS019康复轮椅

官方来源

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