未知设备
PMA编号：P990045 · 2021-12-21
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决定日期2021-12-21
PMA 编号P990045
产品代码
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器械摘要
Unknown Device is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2021-12-21. It was reviewed by the MI advisory panel.
常见问题
What is the Unknown Device?
Unknown Device is a medical device that received FDA 510(k) clearance on 2021-12-21. The listed applicant is DiaSorin, Inc..
When did Unknown Device receive FDA 510(k) clearance?
The clearance date for Unknown Device can be found in the official FDA records.
Who is the listed applicant for Unknown Device?
The FDA 510(k) record lists DiaSorin, Inc. as the applicant. This does not by itself establish the device manufacturer.
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。
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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