iLoop 干预线圈 0.55T
K号: K241069 · 2024-06-07
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器械摘要
iLoop Interventional Coil 0.55T is the device name listed in this FDA 510(k) record. The listed applicant is Noras Mri Products GmbH. It received FDA 510(k) clearance on 2024-06-07 under 510(k) number K241069. 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 iLoop Interventional Coil 0.55T?
iLoop Interventional Coil 0.55T is a medical device that received FDA 510(k) clearance on 2024-06-07. The listed applicant is Noras Mri Products GmbH. The 510(k) number is K241069.
When did iLoop Interventional Coil 0.55T receive FDA 510(k) clearance?
iLoop Interventional Coil 0.55T received FDA 510(k) clearance on 2024-06-07, under 510(k) number K241069.
Who is the listed applicant for iLoop Interventional Coil 0.55T?
The FDA 510(k) record lists Noras Mri Products GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iLoop Interventional Coil 0.55T?
The FDA product code for iLoop Interventional Coil 0.55T is MOS.
相关临床试验
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列明Noras Mri Products GmbH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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