Last synced on 15 September 2023 at 11:04 pm

Synapse Transcutaneous Electrical Stimulation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143198
510(k) Type
Traditional
Applicant
Synapse Electroceutical Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/27/2015
Days to Decision
202 days
Submission Type
Summary

Synapse Transcutaneous Electrical Stimulation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143198
510(k) Type
Traditional
Applicant
Synapse Electroceutical Limited
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/27/2015
Days to Decision
202 days
Submission Type
Summary