LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source
K-Number: K163572 · 2017-03-15
Device Summary
Frequently Asked Questions
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.
Other records listing Lv Liberty Vision Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KXK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.