免疫组织化学检测，抗体，表皮生长因子受体
PMA编号：P030044 · 2019-03-13
广告
决定日期2019-03-13
PMA 编号P030044
产品代码NQF
设备分类第3类
医疗专科H
法规编号21 CFR 8
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
Immunohistochemistry assay, antibody, epidermal growth factor receptor is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2019-03-13. The device is classified under product code NQF. It was reviewed by the PA advisory panel.
常见问题
What is the Immunohistochemistry assay, antibody, epidermal growth factor receptor?
Immunohistochemistry assay, antibody, epidermal growth factor receptor is a medical device that received FDA 510(k) clearance on 2019-03-13. The listed applicant is Agilent Technologies, Inc..
When did Immunohistochemistry assay, antibody, epidermal growth factor receptor receive FDA 510(k) clearance?
The clearance date for Immunohistochemistry assay, antibody, epidermal growth factor receptor can be found in the official FDA records.
Who is the listed applicant for Immunohistochemistry assay, antibody, epidermal growth factor receptor?
The FDA 510(k) record lists Agilent Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Immunohistochemistry assay, antibody, epidermal growth factor receptor?
The FDA product code for Immunohistochemistry assay, antibody, epidermal growth factor receptor is NQF.
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。
广告