Nexcore GI 吸引器
K号: K162332 · 2016-09-29
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决定日期2016-09-29
产品代码FCX
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。
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器械摘要
Nexcore GI Insufflator is the device name listed in this FDA 510(k) record. The listed applicant is Nexcore Technology, LLC. It received FDA 510(k) clearance on 2016-09-29 under 510(k) number K162332. The device is classified under product code FCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nexcore GI Insufflator?
Nexcore GI Insufflator is a medical device that received FDA 510(k) clearance on 2016-09-29. The listed applicant is Nexcore Technology, LLC. The 510(k) number is K162332.
When did Nexcore GI Insufflator receive FDA 510(k) clearance?
Nexcore GI Insufflator received FDA 510(k) clearance on 2016-09-29, under 510(k) number K162332.
Who is the listed applicant for Nexcore GI Insufflator?
The FDA 510(k) record lists Nexcore Technology, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nexcore GI Insufflator?
The FDA product code for Nexcore GI Insufflator is FCX.
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。
相关器械（代码：FCX）
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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