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ClearCorrect System

Page Type
Cleared 510(K)
510(k) Number
K220140
510(k) Type
Traditional
Applicant
ClearCorrect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2022
Days to Decision
260 days
Submission Type
Summary

ClearCorrect System

Page Type
Cleared 510(K)
510(k) Number
K220140
510(k) Type
Traditional
Applicant
ClearCorrect, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2022
Days to Decision
260 days
Submission Type
Summary