FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE

K Number: K072123 · Decision Feb 1, 2008
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
8
Review Days
183

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Basic Information

Device Name
HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE
K Number
K072123
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biowave Corporation
Date Received
August 2, 2007
Decision Date
February 1, 2008
Product Code
GZJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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Other Clearances by Biowave Corporation

K Number Device Name
K261522 BioWave BioWraps
K203158 BioWave BioWraps
K210202 BioWaveGO RX
K180943 BioWaveGO
K152437 BiowaveHOME Neuromodulation Pain Therapy Device
K061166 DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM
K052289 DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE