IRRIGO 创面冲洗喷射系统
K号: K210987 · 2022-05-31
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申请人Inopro, Inc.
决定日期2022-05-31
产品代码FQH
咨询委员会医疗设备监管文本翻译如下：
HO
请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同
器械摘要
IRRIGO Wound Wash Jet System is the device name listed in this FDA 510(k) record. The listed applicant is Inopro, Inc.. It received FDA 510(k) clearance on 2022-05-31 under 510(k) number K210987. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the IRRIGO Wound Wash Jet System?
IRRIGO Wound Wash Jet System is a medical device that received FDA 510(k) clearance on 2022-05-31. The listed applicant is Inopro, Inc.. The 510(k) number is K210987.
When did IRRIGO Wound Wash Jet System receive FDA 510(k) clearance?
IRRIGO Wound Wash Jet System received FDA 510(k) clearance on 2022-05-31, under 510(k) number K210987.
Who is the listed applicant for IRRIGO Wound Wash Jet System?
The FDA 510(k) record lists Inopro, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IRRIGO Wound Wash Jet System?
The FDA product code for IRRIGO Wound Wash Jet System is FQH.
相关临床试验
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相关器械（代码：FQH）
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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