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Sonendo GentleWave System

Page Type
Cleared 510(K)
510(k) Number
K160905
510(k) Type
Special
Applicant
SONENDO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2016
Days to Decision
63 days
Submission Type
Summary

Sonendo GentleWave System

Page Type
Cleared 510(K)
510(k) Number
K160905
510(k) Type
Special
Applicant
SONENDO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2016
Days to Decision
63 days
Submission Type
Summary