FDA 510(k)

LV Liberty Vision Model 1 90Yttrium Brachytherapy Source

Número K: K193602 · 2020-05-29

Data da decisão2020-05-29

Código do produtoKXK

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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