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Stimulator Kit, Trial Kit, Spare Lead Kit, Wearable Assembly Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180981
510(k) Type
Traditional
Applicant
Stimwave Technologies Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2018
Days to Decision
159 days
Submission Type
Summary

Stimulator Kit, Trial Kit, Spare Lead Kit, Wearable Assembly Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180981
510(k) Type
Traditional
Applicant
Stimwave Technologies Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2018
Days to Decision
159 days
Submission Type
Summary