BR-FHUS 观察器 1.0
K号: K171709 · 2017-10-20
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器械摘要
BR-FHUS Viewer 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Taihao Medical, Inc.. It received FDA 510(k) clearance on 2017-10-20 under 510(k) number K171709. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the BR-FHUS Viewer 1.0?
BR-FHUS Viewer 1.0 is a medical device that received FDA 510(k) clearance on 2017-10-20. The listed applicant is Taihao Medical, Inc.. The 510(k) number is K171709.
When did BR-FHUS Viewer 1.0 receive FDA 510(k) clearance?
BR-FHUS Viewer 1.0 received FDA 510(k) clearance on 2017-10-20, under 510(k) number K171709.
Who is the listed applicant for BR-FHUS Viewer 1.0?
The FDA 510(k) record lists Taihao Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BR-FHUS Viewer 1.0?
The FDA product code for BR-FHUS Viewer 1.0 is LLZ.
相关临床试验
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列明Taihao Medical, Inc.为申报人的其他记录
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相关器械（代码：LLZ）
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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