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Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K233804
510(k) Type
Traditional
Applicant
Zeltiq Aesthetics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2024
Days to Decision
64 days
Submission Type
Summary

Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K233804
510(k) Type
Traditional
Applicant
Zeltiq Aesthetics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2024
Days to Decision
64 days
Submission Type
Summary