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PicoWay Laser System

Page Type
Cleared 510(K)
510(k) Number
K162454
510(k) Type
Traditional
Applicant
SYNERON CANDELA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2017
Days to Decision
153 days
Submission Type
Summary

PicoWay Laser System

Page Type
Cleared 510(K)
510(k) Number
K162454
510(k) Type
Traditional
Applicant
SYNERON CANDELA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2017
Days to Decision
153 days
Submission Type
Summary