CoverScan（CoverScan v1.1）
K号: K230294 · 2023-03-03
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器械摘要
CoverScan (CoverScan v1.1) is the device name listed in this FDA 510(k) record. The listed applicant is Perspectum. It received FDA 510(k) clearance on 2023-03-03 under 510(k) number K230294. 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 CoverScan (CoverScan v1.1)?
CoverScan (CoverScan v1.1) is a medical device that received FDA 510(k) clearance on 2023-03-03. The listed applicant is Perspectum. The 510(k) number is K230294.
When did CoverScan (CoverScan v1.1) receive FDA 510(k) clearance?
CoverScan (CoverScan v1.1) received FDA 510(k) clearance on 2023-03-03, under 510(k) number K230294.
Who is the listed applicant for CoverScan (CoverScan v1.1)?
The FDA 510(k) record lists Perspectum as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CoverScan (CoverScan v1.1)?
The FDA product code for CoverScan (CoverScan v1.1) is LLZ.
相关临床试验
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列明Perspectum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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