ViroZap 室内空气净化器，管道式型号 1008
K号: K241140 · 2024-08-01
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决定日期2024-08-01
产品代码FRA
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。
决定实质等同
器械摘要
ViroZap Indoor Air Purifier, In Duct Model 1008 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Photonix, LLC. It received FDA 510(k) clearance on 2024-08-01 under 510(k) number K241140. The device is classified under product code FRA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ViroZap Indoor Air Purifier, In Duct Model 1008?
ViroZap Indoor Air Purifier, In Duct Model 1008 is a medical device that received FDA 510(k) clearance on 2024-08-01. The listed applicant is Applied Photonix, LLC. The 510(k) number is K241140.
When did ViroZap Indoor Air Purifier, In Duct Model 1008 receive FDA 510(k) clearance?
ViroZap Indoor Air Purifier, In Duct Model 1008 received FDA 510(k) clearance on 2024-08-01, under 510(k) number K241140.
Who is the listed applicant for ViroZap Indoor Air Purifier, In Duct Model 1008?
The FDA 510(k) record lists Applied Photonix, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ViroZap Indoor Air Purifier, In Duct Model 1008?
The FDA product code for ViroZap Indoor Air Purifier, In Duct Model 1008 is FRA.
相关临床试验
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相关器械（代码：FRA）
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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