FDA 510(k) Applications Submitted by Matt Farley

FDA 510(k) Number Submission Date Device Name Applicant
K223026 09/29/2022 NES Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter Northeast Scientific, Inc.
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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