Last synced on 14 November 2025 at 11:06 pm

Profound System

Page Type
Cleared 510(K)
510(k) Number
K161043
510(k) Type
Traditional
Applicant
SYNERON CANDELA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2016
Days to Decision
152 days
Submission Type
Summary

Profound System

Page Type
Cleared 510(K)
510(k) Number
K161043
510(k) Type
Traditional
Applicant
SYNERON CANDELA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2016
Days to Decision
152 days
Submission Type
Summary