纤维尘 PRO
K号: K220426 · 2022-03-16
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器械摘要
Fiber Dust PRO is the device name listed in this FDA 510(k) record. The listed applicant is Quanta System Spa. It received FDA 510(k) clearance on 2022-03-16 under 510(k) number K220426. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Fiber Dust PRO?
Fiber Dust PRO is a medical device that received FDA 510(k) clearance on 2022-03-16. The listed applicant is Quanta System Spa. The 510(k) number is K220426.
When did Fiber Dust PRO receive FDA 510(k) clearance?
Fiber Dust PRO received FDA 510(k) clearance on 2022-03-16, under 510(k) number K220426.
Who is the listed applicant for Fiber Dust PRO?
The FDA 510(k) record lists Quanta System Spa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fiber Dust PRO?
The FDA product code for Fiber Dust PRO is GEX. This falls under the Gastroenterology category.
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。
列明Quanta System Spa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：GEX）
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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