Last synced on 10 January 2025 at 11:05 pm

InMode RF Pro System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210492
510(k) Type
Traditional
Applicant
InMode MD Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/12/2021
Days to Decision
143 days
Submission Type
Summary

InMode RF Pro System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210492
510(k) Type
Traditional
Applicant
InMode MD Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/12/2021
Days to Decision
143 days
Submission Type
Summary