FDA 510(k) Applications Submitted by Northeast Scientific, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K090661 03/12/2009 NES REPROCESSED VARICOSE VEIN RF CATHETER Northeast Scientific, Inc.
K060676 03/14/2006 NES REPROCESSED ENDOSCOPIC TROCAR Northeast Scientific, Inc.
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.


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