CORIS 系统
K号: K253267 · 2026-03-05
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决定日期2026-03-05
产品代码SEW
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。
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器械摘要
CORIS System is the device name listed in this FDA 510(k) record. The listed applicant is Nanosonics Limited. It received FDA 510(k) clearance on 2026-03-05 under 510(k) number K253267. The device is classified under product code SEW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CORIS System?
CORIS System is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Nanosonics Limited. The 510(k) number is K253267.
When did CORIS System receive FDA 510(k) clearance?
CORIS System received FDA 510(k) clearance on 2026-03-05, under 510(k) number K253267.
Who is the listed applicant for CORIS System?
The FDA 510(k) record lists Nanosonics Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORIS System?
The FDA product code for CORIS System is SEW.
相关临床试验
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列明Nanosonics Limited为申报人的其他记录
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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