Reach
K号: K170789 · 2017-05-05
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器械摘要
In Reach is the device name listed in this FDA 510(k) record. The listed applicant is Curvebeam, LLC. It received FDA 510(k) clearance on 2017-05-05 under 510(k) number K170789. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the In Reach?
In Reach is a medical device that received FDA 510(k) clearance on 2017-05-05. The listed applicant is Curvebeam, LLC. The 510(k) number is K170789.
When did In Reach receive FDA 510(k) clearance?
In Reach received FDA 510(k) clearance on 2017-05-05, under 510(k) number K170789.
Who is the listed applicant for In Reach?
The FDA 510(k) record lists Curvebeam, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for In Reach?
The FDA product code for In Reach is JAK.
相关临床试验
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列明Curvebeam, LLC为申报人的其他记录
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相关器械（代码：JAK）
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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