处理器，宫颈细胞学切片，自动化
PMA编号：P950039 · 2025-08-27
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决定日期2025-08-27
PMA 编号P950039
产品代码MKQ
设备分类第3类
医疗专科U
咨询委员会PA
请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。
器械摘要
Processor, cervical cytology slide, automated is the device name listed in this FDA 510(k) record. The listed applicant is Hologic, Inc.. It received FDA 510(k) clearance on 2025-08-27. The device is classified under product code MKQ. It was reviewed by the PA advisory panel.
常见问题
What is the Processor, cervical cytology slide, automated?
Processor, cervical cytology slide, automated is a medical device that received FDA 510(k) clearance on 2025-08-27. The listed applicant is Hologic, Inc..
When did Processor, cervical cytology slide, automated receive FDA 510(k) clearance?
The clearance date for Processor, cervical cytology slide, automated can be found in the official FDA records.
Who is the listed applicant for Processor, cervical cytology slide, automated?
FDA 510(k)记录中列出了Hologic, Inc.为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Processor, cervical cytology slide, automated?
The FDA product code for Processor, cervical cytology slide, automated is MKQ.
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。
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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