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TheraFace LED

Page Type
Cleared 510(K)
510(k) Number
K212155
510(k) Type
Traditional
Applicant
Theragun, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2021
Days to Decision
162 days
Submission Type
Summary

TheraFace LED

Page Type
Cleared 510(K)
510(k) Number
K212155
510(k) Type
Traditional
Applicant
Theragun, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2021
Days to Decision
162 days
Submission Type
Summary