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ACTION II Laser System

Page Type
Cleared 510(K)
510(k) Number
K163196
510(k) Type
Traditional
Applicant
LUTRONIC CORPORATION
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/24/2017
Days to Decision
190 days
Submission Type
Summary

ACTION II Laser System

Page Type
Cleared 510(K)
510(k) Number
K163196
510(k) Type
Traditional
Applicant
LUTRONIC CORPORATION
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/24/2017
Days to Decision
190 days
Submission Type
Summary