MagXtract Collection Tube
K号: K212113 · 2022-07-28
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决定日期2022-07-28
产品代码QBD
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器械摘要
MagXtract Collection Tube is the device name listed in this FDA 510(k) record. The listed applicant is Magbio Genomics, Inc.. It received FDA 510(k) clearance on 2022-07-28 under 510(k) number K212113. The device is classified under product code QBD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MagXtract Collection Tube?
MagXtract Collection Tube is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Magbio Genomics, Inc.. The 510(k) number is K212113.
When did MagXtract Collection Tube receive FDA 510(k) clearance?
MagXtract Collection Tube received FDA 510(k) clearance on 2022-07-28, under 510(k) number K212113.
Who is the listed applicant for MagXtract Collection Tube?
The FDA 510(k) record lists Magbio Genomics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MagXtract Collection Tube?
The FDA product code for MagXtract Collection Tube is QBD.
相关临床试验
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相关器械（代码：QBD）
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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