MRCAT 颈部与头部
K号: K214081 · 2022-04-05
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器械摘要
MRCAT Head & Neck is the device name listed in this FDA 510(k) record. The listed applicant is Philips OY. It received FDA 510(k) clearance on 2022-04-05 under 510(k) number K214081. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MRCAT Head & Neck?
MRCAT Head & Neck is a medical device that received FDA 510(k) clearance on 2022-04-05. The listed applicant is Philips OY. The 510(k) number is K214081.
When did MRCAT Head & Neck receive FDA 510(k) clearance?
MRCAT Head & Neck received FDA 510(k) clearance on 2022-04-05, under 510(k) number K214081.
Who is the listed applicant for MRCAT Head & Neck?
The FDA 510(k) record lists Philips OY as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRCAT Head & Neck?
The FDA product code for MRCAT Head & Neck is MUJ.
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：MUJ）
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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