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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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