CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV
K号: K192730 · 2020-09-09
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决定日期2020-09-09
产品代码CHW
咨询委员会CH
请注意，您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV is the device name listed in this FDA 510(k) record. The listed applicant is Biosystems S.A.. It received FDA 510(k) clearance on 2020-09-09 under 510(k) number K192730. The device is classified under product code CHW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV?
CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV is a medical device that received FDA 510(k) clearance on 2020-09-09. The listed applicant is Biosystems S.A.. The 510(k) number is K192730.
When did CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV receive FDA 510(k) clearance?
CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV received FDA 510(k) clearance on 2020-09-09, under 510(k) number K192730.
Who is the listed applicant for CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV?
The FDA 510(k) record lists Biosystems S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV?
The FDA product code for CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UV is CHW.
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。
列明Biosystems S.A.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。
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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