FDA 510(k) Applications Submitted by BioWave Corporation

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
K061166	04/27/2006	DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM	BIOWAVE CORPORATION
K072123	08/02/2007	HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE	BIOWAVE CORPORATION
K052289	08/23/2005	DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE	BIOWAVE CORPORATION