Last synced on 14 November 2025 at 11:06 pm

Thermeo System

Page Type
Cleared 510(K)
510(k) Number
K212017
510(k) Type
Traditional
Applicant
Pro3dure Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/8/2022
Days to Decision
284 days
Submission Type
Summary

Thermeo System

Page Type
Cleared 510(K)
510(k) Number
K212017
510(k) Type
Traditional
Applicant
Pro3dure Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/8/2022
Days to Decision
284 days
Submission Type
Summary