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FDA 510(k)

LV Liberty Vision Model 1 90Yttrium Brachytherapy Source

K-Number: K193602 · 2020-05-29

ApplicantLv Liberty Vision Corporation
Decision Date2020-05-29
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LV Liberty Vision Model 1 90Yttrium Brachytherapy Source is a medical device manufactured by Lv Liberty Vision Corporation. It received FDA 510(k) clearance on 2020-05-29 under approval number K193602. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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. It is manufactured by Lv Liberty Vision Corporation. The 510(k) number is K193602.

When was LV Liberty Vision Model 1 90Yttrium Brachytherapy Source approved by the FDA?

LV Liberty Vision Model 1 90Yttrium Brachytherapy Source received FDA 510(k) clearance on 2020-05-29, under approval number K193602.

What company makes LV Liberty Vision Model 1 90Yttrium Brachytherapy Source?

LV Liberty Vision Model 1 90Yttrium Brachytherapy Source is manufactured by Lv Liberty Vision Corporation.

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.

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Related Devices (Code: KXK)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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