Giraffe Omnibed 护理站 CS1
K号: K213551 · 2022-03-02
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决定日期2022-03-02
产品代码FMT
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。
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器械摘要
Giraffe Omnibed Carestation CS1 is the device name listed in this FDA 510(k) record. The listed applicant is Datex Ohmeda, Inc.. It received FDA 510(k) clearance on 2022-03-02 under 510(k) number K213551. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Giraffe Omnibed Carestation CS1?
Giraffe Omnibed Carestation CS1 is a medical device that received FDA 510(k) clearance on 2022-03-02. The listed applicant is Datex Ohmeda, Inc.. The 510(k) number is K213551.
When did Giraffe Omnibed Carestation CS1 receive FDA 510(k) clearance?
Giraffe Omnibed Carestation CS1 received FDA 510(k) clearance on 2022-03-02, under 510(k) number K213551.
Who is the listed applicant for Giraffe Omnibed Carestation CS1?
FDA 510(k)记录中列出Datex Ohmeda, Inc.为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Giraffe Omnibed Carestation CS1?
The FDA product code for Giraffe Omnibed Carestation CS1 is FMT.
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Datex Ohmeda, 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：FMT）
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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