URO-TOUCH 9 法式探头
K号: K202813 · 2021-06-14
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决定日期2021-06-14
产品代码FFK
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同
器械摘要
URO-TOUCH 9 French Probe is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 2021-06-14 under 510(k) number K202813. The device is classified under product code FFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the URO-TOUCH 9 French Probe?
URO-TOUCH 9 French Probe is a medical device that received FDA 510(k) clearance on 2021-06-14. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K202813.
When did URO-TOUCH 9 French Probe receive FDA 510(k) clearance?
URO-TOUCH 9 French Probe received FDA 510(k) clearance on 2021-06-14, under 510(k) number K202813.
Who is the listed applicant for URO-TOUCH 9 French Probe?
The FDA 510(k) record lists Northgate Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URO-TOUCH 9 French Probe?
The FDA product code for URO-TOUCH 9 French Probe is FFK.
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Northgate Technologies, 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：FFK）
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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