3543A、4343A、2929A 和 A843B 型号
K号: K170480 · 2017-07-07
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器械摘要
Models 3543A, 4343A, 2929A and A843B is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai PZ Medical Technolgoy Co., Ltd.. It received FDA 510(k) clearance on 2017-07-07 under 510(k) number K170480. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Models 3543A, 4343A, 2929A and A843B?
Models 3543A, 4343A, 2929A and A843B is a medical device that received FDA 510(k) clearance on 2017-07-07. The listed applicant is Shanghai PZ Medical Technolgoy Co., Ltd.. The 510(k) number is K170480.
When did Models 3543A, 4343A, 2929A and A843B receive FDA 510(k) clearance?
Models 3543A, 4343A, 2929A and A843B received FDA 510(k) clearance on 2017-07-07, under 510(k) number K170480.
Who is the listed applicant for Models 3543A, 4343A, 2929A and A843B?
The FDA 510(k) record lists Shanghai PZ Medical Technolgoy Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Models 3543A, 4343A, 2929A and A843B?
The FDA product code for Models 3543A, 4343A, 2929A and A843B is MQB.
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：MQB）
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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