系统，高温，射频/微波（良性前列腺增生），热疗
PMA编号：P030006 · 2018-11-21
广告
决定日期2018-11-21
PMA 编号P030006
产品代码MEQ
设备分类第3类
医疗专科U
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
器械摘要
System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy is the device name listed in this FDA 510(k) record. The listed applicant is Medifocus, Inc.. It received FDA 510(k) clearance on 2018-11-21. The device is classified under product code MEQ. It was reviewed by the GU advisory panel.
常见问题
What is the System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy?
System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy is a medical device that received FDA 510(k) clearance on 2018-11-21. The listed applicant is Medifocus, Inc..
When did System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy receive FDA 510(k) clearance?
The clearance date for System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy can be found in the official FDA records.
Who is the listed applicant for System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy?
The FDA 510(k) record lists Medifocus, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy?
The FDA product code for System, hyperthermia, rf/microwave (benign prostatic hyperplasia),thermotherapy is MEQ.
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