Precision GI
K号: K231422 · 2023-08-28
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决定日期2023-08-28
产品代码FCG
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
Precision GI is the device name listed in this FDA 510(k) record. The listed applicant is Limaca Medical, Ltd.. It received FDA 510(k) clearance on 2023-08-28 under 510(k) number K231422. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Precision GI?
Precision GI is a medical device that received FDA 510(k) clearance on 2023-08-28. The listed applicant is Limaca Medical, Ltd.. The 510(k) number is K231422.
When did Precision GI receive FDA 510(k) clearance?
Precision GI received FDA 510(k) clearance on 2023-08-28, under 510(k) number K231422.
Who is the listed applicant for Precision GI?
The FDA 510(k) record lists Limaca Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Precision GI?
The FDA product code for Precision GI is FCG.
相关临床试验
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相关器械（代码：FCG）
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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