Scanostics UTI Check应用程序测试系统
K号: K170118 · 2017-09-21
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决定日期2017-09-21
产品代码JMT
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。
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器械摘要
Scanostics UTI Check Application Test System is the device name listed in this FDA 510(k) record. The listed applicant is Teco Diagnostics. It received FDA 510(k) clearance on 2017-09-21 under 510(k) number K170118. The device is classified under product code JMT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Scanostics UTI Check Application Test System?
Scanostics UTI Check Application Test System is a medical device that received FDA 510(k) clearance on 2017-09-21. The listed applicant is Teco Diagnostics. The 510(k) number is K170118.
When did Scanostics UTI Check Application Test System receive FDA 510(k) clearance?
Scanostics UTI Check Application Test System received FDA 510(k) clearance on 2017-09-21, under 510(k) number K170118.
Who is the listed applicant for Scanostics UTI Check Application Test System?
The FDA 510(k) record lists Teco Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Scanostics UTI Check Application Test System?
The FDA product code for Scanostics UTI Check Application Test System is JMT.
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相关器械（代码：JMT）
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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