NewTom VGi evo
K号: K151612 · 2016-03-31
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器械摘要
NewTom VGi evo is the device name listed in this FDA 510(k) record. The listed applicant is Qr S.R.L.. It received FDA 510(k) clearance on 2016-03-31 under 510(k) number K151612. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NewTom VGi evo?
NewTom VGi evo is a medical device that received FDA 510(k) clearance on 2016-03-31. The listed applicant is Qr S.R.L.. The 510(k) number is K151612.
When did NewTom VGi evo receive FDA 510(k) clearance?
NewTom VGi evo received FDA 510(k) clearance on 2016-03-31, under 510(k) number K151612.
Who is the listed applicant for NewTom VGi evo?
The FDA 510(k) record lists Qr S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NewTom VGi evo?
The FDA product code for NewTom VGi evo is OAS.
相关临床试验
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相关器械（代码：OAS）
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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