Last synced on 21 June 2024 at 11:04 pm

Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, Wearable Antenna Assembly Kit and Charger Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170141
510(k) Type
Traditional
Applicant
Stimwave Technologies Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2017
Days to Decision
105 days
Submission Type
Summary

Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, Wearable Antenna Assembly Kit and Charger Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170141
510(k) Type
Traditional
Applicant
Stimwave Technologies Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2017
Days to Decision
105 days
Submission Type
Summary