EndoSign® 细胞采集装置 (ES-CYT-102)
K号: K233142 · 2024-01-19
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决定日期2024-01-19
产品代码EOX
咨询委员会医疗设备监管文本描述翻译如下：
关于[公司/产品名称]的监管信息：
- 美国食品药品监督管理局（FDA）批准号：[510(k)编号]
- 预市场批准（PMA）申请号：[PMA编号]
- 临床试验注册号（NCT）：[NCT编号]
- 医学文献标识符（PMID）：[PMID编号]
- 产品标识符：[标识符]
- 相关政策：医疗监管政策v1
- 更多信息请访问：[URL]
请注意，以上翻译保留了公司/产品名称、FDA、510(k)、PMA、NCT、PMID、标识符和URL。
决定实质等同
器械摘要
EndoSign® Cell collection device (ES-CYT-102) is the device name listed in this FDA 510(k) record. The listed applicant is Cyted Limited. It received FDA 510(k) clearance on 2024-01-19 under 510(k) number K233142. The device is classified under product code EOX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the EndoSign® Cell collection device (ES-CYT-102)?
EndoSign® Cell collection device (ES-CYT-102) is a medical device that received FDA 510(k) clearance on 2024-01-19. The listed applicant is Cyted Limited. The 510(k) number is K233142.
When did EndoSign® Cell collection device (ES-CYT-102) receive FDA 510(k) clearance?
EndoSign® Cell collection device (ES-CYT-102) received FDA 510(k) clearance on 2024-01-19, under 510(k) number K233142.
Who is the listed applicant for EndoSign® Cell collection device (ES-CYT-102)?
The FDA 510(k) record lists Cyted Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EndoSign® Cell collection device (ES-CYT-102)?
The FDA product code for EndoSign® Cell collection device (ES-CYT-102) is EOX.
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：EOX）
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。
K230339EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K223072PENTAX 医疗视频食管镜 EE17-J10Pentax of America, Inc.K222366EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K203450EsophaCap 可吞咽性细胞回收装置（从Cell-Mata更名）Capnostics, LLCK210137EsoCheck Cell Collection DeviceLucid Diagnostics, Inc.K192523CMOS 视频食管镜 SSUKarl Storz SE & CO. KG
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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