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Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K210964
510(k) Type
Special
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2021
Days to Decision
27 days
Submission Type
Summary

Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K210964
510(k) Type
Special
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2021
Days to Decision
27 days
Submission Type
Summary