DizzyDoctor 系统 1.0.0
K号: K182214 · 2018-09-14
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决定日期2018-09-14
产品代码GWN
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
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器械摘要
DizzyDoctor System 1.0.0 is the device name listed in this FDA 510(k) record. The listed applicant is Dizzydoctor Systems, LLC. It received FDA 510(k) clearance on 2018-09-14 under 510(k) number K182214. The device is classified under product code GWN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DizzyDoctor System 1.0.0?
DizzyDoctor System 1.0.0 is a medical device that received FDA 510(k) clearance on 2018-09-14. The listed applicant is Dizzydoctor Systems, LLC. The 510(k) number is K182214.
When did DizzyDoctor System 1.0.0 receive FDA 510(k) clearance?
DizzyDoctor System 1.0.0 received FDA 510(k) clearance on 2018-09-14, under 510(k) number K182214.
Who is the listed applicant for DizzyDoctor System 1.0.0?
The FDA 510(k) record lists Dizzydoctor Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DizzyDoctor System 1.0.0?
The FDA product code for DizzyDoctor System 1.0.0 is GWN.
相关临床试验
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相关器械（代码：GWN）
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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