MD-Temp Plus
K号: K190724 · 2019-07-03
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决定日期2019-07-03
产品代码EBG
咨询委员会DE
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决定实质等同
器械摘要
MD-Temp Plus is the device name listed in this FDA 510(k) record. The listed applicant is Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2019-07-03 under 510(k) number K190724. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MD-Temp Plus?
MD-Temp Plus is a medical device that received FDA 510(k) clearance on 2019-07-03. The listed applicant is Meta Biomed Co., Ltd.. The 510(k) number is K190724.
When did MD-Temp Plus receive FDA 510(k) clearance?
MD-Temp Plus received FDA 510(k) clearance on 2019-07-03, under 510(k) number K190724.
Who is the listed applicant for MD-Temp Plus?
The FDA 510(k) record lists Meta Biomed Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MD-Temp Plus?
The FDA product code for MD-Temp Plus is EBG.
列明Meta Biomed Co., Ltd.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：EBG）
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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