系统，激光，光动力治疗
PMA编号：P050026 · 2025-02-11
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决定日期2025-02-11
PMA 编号P050026
产品代码MVF
设备分类第3类
医疗专科U
咨询委员会OP
请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。
器械摘要
System, laser, photodynamic therapy is the device name listed in this FDA 510(k) record. The listed applicant is Bausch + Lomb Ireland Limited. It received FDA 510(k) clearance on 2025-02-11. The device is classified under product code MVF. It was reviewed by the OP advisory panel.
常见问题
What is the System, laser, photodynamic therapy?
System, laser, photodynamic therapy is a medical device that received FDA 510(k) clearance on 2025-02-11. The listed applicant is Bausch + Lomb Ireland Limited.
When did System, laser, photodynamic therapy receive FDA 510(k) clearance?
The clearance date for System, laser, photodynamic therapy can be found in the official FDA records.
Who is the listed applicant for System, laser, photodynamic therapy?
The FDA 510(k) record lists Bausch + Lomb Ireland Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for System, laser, photodynamic therapy?
The FDA product code for System, laser, photodynamic therapy is MVF.
相关临床试验
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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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