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REVITIVE IX

Page Type
Cleared 510(K)
510(k) Number
K123354
510(k) Type
Traditional
Applicant
Actegy Ltd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2013
Days to Decision
240 days
Submission Type
Summary

REVITIVE IX

Page Type
Cleared 510(K)
510(k) Number
K123354
510(k) Type
Traditional
Applicant
Actegy Ltd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2013
Days to Decision
240 days
Submission Type
Summary