LightLas多波长医疗激光系统
K号: K152688 · 2016-06-15
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决定日期2016-06-15
产品代码HQF
咨询委员会OP
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决定实质等同
器械摘要
LightLas Multi-Wavelength Medical Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Lightmed Corporation. It received FDA 510(k) clearance on 2016-06-15 under 510(k) number K152688. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LightLas Multi-Wavelength Medical Laser System?
LightLas Multi-Wavelength Medical Laser System is a medical device that received FDA 510(k) clearance on 2016-06-15. The listed applicant is Lightmed Corporation. The 510(k) number is K152688.
When did LightLas Multi-Wavelength Medical Laser System receive FDA 510(k) clearance?
LightLas Multi-Wavelength Medical Laser System received FDA 510(k) clearance on 2016-06-15, under 510(k) number K152688.
Who is the listed applicant for LightLas Multi-Wavelength Medical Laser System?
The FDA 510(k) record lists Lightmed Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LightLas Multi-Wavelength Medical Laser System?
The FDA product code for LightLas Multi-Wavelength Medical Laser System is HQF.
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相关器械（代码：HQF）
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。
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