TrabEx Pro
K号: K213173 · 2022-06-08
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决定日期2022-06-08
产品代码MRH
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
TrabEx Pro is the device name listed in this FDA 510(k) record. The listed applicant is Microsurgical Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-08 under 510(k) number K213173. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the TrabEx Pro?
TrabEx Pro is a medical device that received FDA 510(k) clearance on 2022-06-08. The listed applicant is Microsurgical Technologies, Inc.. The 510(k) number is K213173.
When did TrabEx Pro receive FDA 510(k) clearance?
TrabEx Pro received FDA 510(k) clearance on 2022-06-08, under 510(k) number K213173.
Who is the listed applicant for TrabEx Pro?
The FDA 510(k) record lists Microsurgical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TrabEx Pro?
The FDA product code for TrabEx Pro is MRH.
相关临床试验
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相关器械（代码：MRH）
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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