E-COM DR-2000 DR
K号: K193644 · 2020-02-14
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器械摘要
E-COM DR-2000 DR is the device name listed in this FDA 510(k) record. The listed applicant is Livermoretech, Inc.. It received FDA 510(k) clearance on 2020-02-14 under 510(k) number K193644. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the E-COM DR-2000 DR?
E-COM DR-2000 DR is a medical device that received FDA 510(k) clearance on 2020-02-14. The listed applicant is Livermoretech, Inc.. The 510(k) number is K193644.
When did E-COM DR-2000 DR receive FDA 510(k) clearance?
E-COM DR-2000 DR received FDA 510(k) clearance on 2020-02-14, under 510(k) number K193644.
Who is the listed applicant for E-COM DR-2000 DR?
The FDA 510(k) record lists Livermoretech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E-COM DR-2000 DR?
The FDA product code for E-COM DR-2000 DR is MQB.
列明Livermoretech, 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：MQB）
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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