IMPLANT，抗胃食管反流
PMA编号：P250018 · 2026-08-20
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决定日期2026-08-20
PMA 编号P250018
产品代码LEI
设备分类第3类
医疗专科U
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。
器械摘要
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX is the device name listed in this FDA 510(k) record. The listed applicant is Implantica CE Reflux , Ltd.. It received FDA 510(k) clearance on 2026-08-20. The device is classified under product code LEI. It was reviewed by the GU advisory panel.
常见问题
What is the IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX?
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX is a medical device that received FDA 510(k) clearance on 2026-08-20. The listed applicant is Implantica CE Reflux , Ltd..
When did IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX receive FDA 510(k) clearance?
The clearance date for IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX can be found in the official FDA records.
谁是IMPLANT，抗胃食管反流产品的列名申请人？
The FDA 510(k) record lists Implantica CE Reflux , Ltd. as the applicant. This does not by itself establish the device manufacturer.
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX 的 FDA 产品代码是什么？
FDA产品代码为IMPLANT，反胃食管反流产品的代码是LEI。
相关临床试验
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官方来源
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