InkSpace 成像小型体阵列
K号: K243675 · 2024-12-20
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器械摘要
InkSpace Imaging Small Body Array is the device name listed in this FDA 510(k) record. The listed applicant is Inkspace Imaging, Inc.. It received FDA 510(k) clearance on 2024-12-20 under 510(k) number K243675. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the InkSpace Imaging Small Body Array?
InkSpace Imaging Small Body Array is a medical device that received FDA 510(k) clearance on 2024-12-20. The listed applicant is Inkspace Imaging, Inc.. The 510(k) number is K243675.
When did InkSpace Imaging Small Body Array receive FDA 510(k) clearance?
InkSpace Imaging Small Body Array received FDA 510(k) clearance on 2024-12-20, under 510(k) number K243675.
Who is the listed applicant for InkSpace Imaging Small Body Array?
The FDA 510(k) record lists Inkspace Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InkSpace Imaging Small Body Array?
The FDA product code for InkSpace Imaging Small Body Array is MOS.
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Inkspace Imaging, Inc.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：MOS）
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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