免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA PMA

READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED

PMA编号:P950009 · 2022-07-11

决定日期2022-07-11
PMA 编号P950009
产品代码MNM
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

READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED is the device name listed in this FDA 510(k) record. The listed applicant is Bd Diagnostics. It received FDA 510(k) clearance on 2022-07-11. The device is classified under product code MNM. It was reviewed by the PA advisory panel.

常见问题

What is the READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED?

READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED is a medical device that received FDA 510(k) clearance on 2022-07-11. The listed applicant is Bd Diagnostics.

When did READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED receive FDA 510(k) clearance?

The clearance date for READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED can be found in the official FDA records.

Who is the listed applicant for READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED?

The FDA 510(k) record lists Bd Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED?

The FDA product code for READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED is MNM.

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。

↑