Last synced on 23 September 2022 at 11:05 pm

PainKARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151034
510(k) Type
Traditional
Applicant
TrioWave Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2015
Days to Decision
218 days
Submission Type
Summary

PainKARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151034
510(k) Type
Traditional
Applicant
TrioWave Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2015
Days to Decision
218 days
Submission Type
Summary