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Thermeo System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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