Scenaria View 4.2
K号: K231574 · 2023-10-12
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器械摘要
Scenaria View 4.2 is the device name listed in this FDA 510(k) record. The listed applicant is FUJIFILM Healthcare Americas Corporation. It received FDA 510(k) clearance on 2023-10-12 under 510(k) number K231574. 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 Scenaria View 4.2?
Scenaria View 4.2 is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is FUJIFILM Healthcare Americas Corporation. The 510(k) number is K231574.
When did Scenaria View 4.2 receive FDA 510(k) clearance?
Scenaria View 4.2 received FDA 510(k) clearance on 2023-10-12, under 510(k) number K231574.
Who is the listed applicant for Scenaria View 4.2?
The FDA 510(k) record lists FUJIFILM Healthcare Americas Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Scenaria View 4.2?
The FDA product code for Scenaria View 4.2 is JAK.
相关临床试验
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列明FUJIFILM Healthcare Americas Corporation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：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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