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Thermi Reusable Non-invasive RF Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171094
510(k) Type
Traditional
Applicant
ThermGen, L.L.C
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2017
Days to Decision
26 days
Submission Type
Summary

Thermi Reusable Non-invasive RF Electrode

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171094
510(k) Type
Traditional
Applicant
ThermGen, L.L.C
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2017
Days to Decision
26 days
Submission Type
Summary