d-Nav 系统
K号: K181916 · 2019-02-04
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决定日期2019-02-04
产品代码NDC
咨询委员会AN
请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。
决定实质等同
器械摘要
d-Nav System is the device name listed in this FDA 510(k) record. The listed applicant is Hygieia, Inc.. It received FDA 510(k) clearance on 2019-02-04 under 510(k) number K181916. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the d-Nav System?
d-Nav System is a medical device that received FDA 510(k) clearance on 2019-02-04. The listed applicant is Hygieia, Inc.. The 510(k) number is K181916.
When did d-Nav System receive FDA 510(k) clearance?
d-Nav System received FDA 510(k) clearance on 2019-02-04, under 510(k) number K181916.
Who is the listed applicant for d-Nav System?
The FDA 510(k) record lists Hygieia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for d-Nav System?
The FDA product code for d-Nav System is NDC.
相关临床试验
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相关器械（代码：NDC）
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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