Colonic Plus常规、小号和直形水套
K号: K180800 · 2018-06-01
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申请人Colonic Plus
决定日期2018-06-01
产品代码KPL
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Unknown
器械摘要
Colonic Plus Regular, Small, and Straight Shape Hydrokit is the device name listed in this FDA 510(k) record. The listed applicant is Colonic Plus. It received FDA 510(k) clearance on 2018-06-01 under 510(k) number K180800. The device is classified under product code KPL. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常见问题
What is the Colonic Plus Regular, Small, and Straight Shape Hydrokit?
Colonic Plus Regular, Small, and Straight Shape Hydrokit is a medical device that received FDA 510(k) clearance on 2018-06-01. The listed applicant is Colonic Plus. The 510(k) number is K180800.
When did Colonic Plus Regular, Small, and Straight Shape Hydrokit receive FDA 510(k) clearance?
Colonic Plus Regular, Small, and Straight Shape Hydrokit received FDA 510(k) clearance on 2018-06-01, under 510(k) number K180800.
Who is the listed applicant for Colonic Plus Regular, Small, and Straight Shape Hydrokit?
The FDA 510(k) record lists Colonic Plus as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Colonic Plus Regular, Small, and Straight Shape Hydrokit?
The FDA product code for Colonic Plus Regular, Small, and Straight Shape Hydrokit is KPL.
相关临床试验
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相关器械（代码：KPL）
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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