植入式可编程输注泵
PMA编号：P800036 · 2020-02-07
广告
决定日期2020-02-07
PMA 编号P800036
产品代码LKK
设备分类第3类
医疗专科U
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。
器械摘要
Pump, infusion, implanted, programmable is the device name listed in this FDA 510(k) record. The listed applicant is Intera Oncology. It received FDA 510(k) clearance on 2020-02-07. The device is classified under product code LKK. It was reviewed by the HO advisory panel.
常见问题
What is the Pump, infusion, implanted, programmable?
Pump, infusion, implanted, programmable is a medical device that received FDA 510(k) clearance on 2020-02-07. The listed applicant is Intera Oncology.
When did Pump, infusion, implanted, programmable receive FDA 510(k) clearance?
The clearance date for Pump, infusion, implanted, programmable can be found in the official FDA records.
泵、输液、植入式、可编程的列名申请人是谁？
The FDA 510(k) record lists Intera Oncology as the applicant. This does not by itself establish the device manufacturer.
什么是泵，植入式，可编程输注产品的FDA产品代码？
FDA产品代码为植入式、可编程泵的代码是LKK。
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