Last synced on 4 February 2023 at 10:33 pm

IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060975
510(k) Type
Special
Applicant
THERATECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2006
Days to Decision
30 days
Submission Type
Summary

IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060975
510(k) Type
Special
Applicant
THERATECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2006
Days to Decision
30 days
Submission Type
Summary