3.0T 16通道AIR AA
K号: K223378 · 2023-01-03
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器械摘要
3.0T 16ch AIR AA is the device name listed in this FDA 510(k) record. The listed applicant is Ge Healthcare Coils (Usa Instruments, Inc.). It received FDA 510(k) clearance on 2023-01-03 under 510(k) number K223378. 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 3.0T 16ch AIR AA?
3.0T 16ch AIR AA is a medical device that received FDA 510(k) clearance on 2023-01-03. The listed applicant is Ge Healthcare Coils (Usa Instruments, Inc.). The 510(k) number is K223378.
When did 3.0T 16ch AIR AA receive FDA 510(k) clearance?
3.0T 16ch AIR AA received FDA 510(k) clearance on 2023-01-03, under 510(k) number K223378.
Who is the listed applicant for 3.0T 16ch AIR AA?
The FDA 510(k) record lists Ge Healthcare Coils (Usa Instruments, Inc.) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3.0T 16ch AIR AA?
The FDA product code for 3.0T 16ch AIR AA is MOS.
列明Ge Healthcare Coils (Usa Instruments, 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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