Encompass 15 Channel Head Coil, 3T
K号: K190668 · 2019-09-09
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器械摘要
Encompass 15 Channel Head Coil, 3T is the device name listed in this FDA 510(k) record. The listed applicant is Qfix. It received FDA 510(k) clearance on 2019-09-09 under 510(k) number K190668. 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 Encompass 15 Channel Head Coil, 3T?
Encompass 15 Channel Head Coil, 3T is a medical device that received FDA 510(k) clearance on 2019-09-09. The listed applicant is Qfix. The 510(k) number is K190668.
When did Encompass 15 Channel Head Coil, 3T receive FDA 510(k) clearance?
Encompass 15 Channel Head Coil, 3T received FDA 510(k) clearance on 2019-09-09, under 510(k) number K190668.
Who is the listed applicant for Encompass 15 Channel Head Coil, 3T?
The FDA 510(k) record lists Qfix as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Encompass 15 Channel Head Coil, 3T?
The FDA product code for Encompass 15 Channel Head Coil, 3T is MOS.
相关临床试验
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列明Qfix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
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