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BiowaveHOME Neuromodulation Pain Therapy Device

Page Type
Cleared 510(K)
510(k) Number
K152437
510(k) Type
Special
Applicant
BIOWAVE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2015
Days to Decision
29 days
Submission Type
Summary

BiowaveHOME Neuromodulation Pain Therapy Device

Page Type
Cleared 510(K)
510(k) Number
K152437
510(k) Type
Special
Applicant
BIOWAVE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2015
Days to Decision
29 days
Submission Type
Summary