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FDA 510(k) Applications Submitted by Paul T. Finger
FDA 510(k) Number
Submission Date
Device Name
Applicant
K163572
12/19/2016
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source
LV Liberty Vision Corp.
K193602
12/23/2019
LV Liberty Vision Model 1 90Yttrium Brachytherapy Source
LV Liberty Vision Corporation
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