多光谱成像套件（MSI套件）(300-00015)，多光谱成像仪（MSI）(300-00009)
K号: K230734 · 2023-12-05
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器械摘要
常见问题
What is the Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009)?
Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009) is a medical device that received FDA 510(k) clearance on 2023-12-05. The listed applicant is Precision Healing, LLC. The 510(k) number is K230734.
When did Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009) receive FDA 510(k) clearance?
Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009) received FDA 510(k) clearance on 2023-12-05, under 510(k) number K230734.
Who is the listed applicant for Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009)?
The FDA 510(k) record lists Precision Healing, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009)?
The FDA product code for Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009) is QJF.
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。
相关器械（代码：QJF）
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。
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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