BAROnova 访问鞘套件
K号: K191078 · 2019-07-22
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决定日期2019-07-22
产品代码QGG
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定Unknown
器械摘要
BAROnova Access Sheath Kit is the device name listed in this FDA 510(k) record. The listed applicant is Baronova, Inc.. It received FDA 510(k) clearance on 2019-07-22 under 510(k) number K191078. The device is classified under product code QGG. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常见问题
What is the BAROnova Access Sheath Kit?
BAROnova Access Sheath Kit is a medical device that received FDA 510(k) clearance on 2019-07-22. The listed applicant is Baronova, Inc.. The 510(k) number is K191078.
When did BAROnova Access Sheath Kit receive FDA 510(k) clearance?
BAROnova Access Sheath Kit received FDA 510(k) clearance on 2019-07-22, under 510(k) number K191078.
Who is the listed applicant for BAROnova Access Sheath Kit?
The FDA 510(k) record lists Baronova, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BAROnova Access Sheath Kit?
The FDA product code for BAROnova Access Sheath Kit is QGG.
相关临床试验
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列明Baronova, 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。
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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