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FDA 510(k) Applications Submitted by Matthew Farley
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220171
01/21/2022
NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter
Northeast Scientific, Inc.
K200195
01/27/2020
NES Reprocessed Visions PV .014P RX Digital IVUS Catheter
Northeast Scientific, Inc.
K173214
10/02/2017
NES Reprocessed RF Stylet (RFS)
Northeast Scientific, Inc. (NES)
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