LV Liberty Vision Model 1 90 钇钴治疗源
K号: K163572 · 2017-03-15
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器械摘要
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source is the device name listed in this FDA 510(k) record. The listed applicant is Lv Liberty Vision Corp.. It received FDA 510(k) clearance on 2017-03-15 under 510(k) number K163572. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source?
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source is a medical device that received FDA 510(k) clearance on 2017-03-15. The listed applicant is Lv Liberty Vision Corp.. The 510(k) number is K163572.
When did LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source receive FDA 510(k) clearance?
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source received FDA 510(k) clearance on 2017-03-15, under 510(k) number K163572.
Who is the listed applicant for LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source?
The FDA 510(k) record lists Lv Liberty Vision Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source?
The FDA product code for LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source is KXK.
相关临床试验
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相关器械（代码：KXK）
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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