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BiowaveHOME Neuromodulation Pain Therapy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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