LV Liberty Vision Model 1 90Y 钇钴治疗源
K号: K193602 · 2020-05-29
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器械摘要
LV Liberty Vision Model 1 90Yttrium Brachytherapy Source is the device name listed in this FDA 510(k) record. The listed applicant is Lv Liberty Vision Corporation. It received FDA 510(k) clearance on 2020-05-29 under 510(k) number K193602. 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 90Yttrium Brachytherapy Source?
LV Liberty Vision Model 1 90Yttrium Brachytherapy Source is a medical device that received FDA 510(k) clearance on 2020-05-29. The listed applicant is Lv Liberty Vision Corporation. The 510(k) number is K193602.
When did LV Liberty Vision Model 1 90Yttrium Brachytherapy Source receive FDA 510(k) clearance?
LV Liberty Vision Model 1 90Yttrium Brachytherapy Source received FDA 510(k) clearance on 2020-05-29, under 510(k) number K193602.
Who is the listed applicant for LV Liberty Vision Model 1 90Yttrium Brachytherapy Source?
The FDA 510(k) record lists Lv Liberty Vision Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LV Liberty Vision Model 1 90Yttrium Brachytherapy Source?
The FDA product code for LV Liberty Vision Model 1 90Yttrium 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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