Last synced on 22 September 2023 at 11:04 pm

HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072123
510(k) Type
Traditional
Applicant
BIOWAVE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2008
Days to Decision
183 days
Submission Type
Summary

HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072123
510(k) Type
Traditional
Applicant
BIOWAVE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2008
Days to Decision
183 days
Submission Type
Summary