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FDA 510(k) Applications Submitted by BRADFORD SIFF
FDA 510(k) Number
Submission Date
Device Name
Applicant
K210202
01/25/2021
BioWaveGO RX
BioWave Corporation
K180943
04/10/2018
BioWaveGO
Biowave Corporation
K152437
08/27/2015
BiowaveHOME Neuromodulation Pain Therapy Device
BIOWAVE CORPORATION
K203158
10/22/2020
BioWave BioWraps
BioWave Corporation
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