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Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K222629
510(k) Type
Traditional
Applicant
Zeltiq Aesthetics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2022
Days to Decision
25 days
Submission Type
Summary

Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K222629
510(k) Type
Traditional
Applicant
Zeltiq Aesthetics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2022
Days to Decision
25 days
Submission Type
Summary