多模态工作站
K号: K192519 · 2019-11-27
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决定日期2019-11-27
产品代码ONF
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Multi-modality workstation is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Superlaser Technology Co., Ltd.. It received FDA 510(k) clearance on 2019-11-27 under 510(k) number K192519. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Multi-modality workstation?
Multi-modality workstation is a medical device that received FDA 510(k) clearance on 2019-11-27. The listed applicant is Beijing Superlaser Technology Co., Ltd.. The 510(k) number is K192519.
When did Multi-modality workstation receive FDA 510(k) clearance?
Multi-modality workstation received FDA 510(k) clearance on 2019-11-27, under 510(k) number K192519.
Who is the listed applicant for Multi-modality workstation?
The FDA 510(k) record lists Beijing Superlaser Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Multi-modality workstation?
The FDA product code for Multi-modality workstation is ONF.
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。
列明Beijing Superlaser Technology Co., Ltd.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：ONF）
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。
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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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