ThermPix 热视像相机
K号: K232462 · 2023-09-14
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决定日期2023-09-14
产品代码LHQ
咨询委员会OB
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决定实质等同
器械摘要
ThermPix Thermovisual Camera is the device name listed in this FDA 510(k) record. The listed applicant is Usa Therm, Inc.. It received FDA 510(k) clearance on 2023-09-14 under 510(k) number K232462. The device is classified under product code LHQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ThermPix Thermovisual Camera?
ThermPix Thermovisual Camera is a medical device that received FDA 510(k) clearance on 2023-09-14. The listed applicant is Usa Therm, Inc.. The 510(k) number is K232462.
When did ThermPix Thermovisual Camera receive FDA 510(k) clearance?
ThermPix Thermovisual Camera received FDA 510(k) clearance on 2023-09-14, under 510(k) number K232462.
Who is the listed applicant for ThermPix Thermovisual Camera?
The FDA 510(k) record lists Usa Therm, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ThermPix Thermovisual Camera?
The FDA product code for ThermPix Thermovisual Camera is LHQ.
相关临床试验
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列明Usa Therm, Inc.为申报人的其他记录
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。
相关器械（代码：LHQ）
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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