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Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212502
510(k) Type
Traditional
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2021
Days to Decision
88 days
Submission Type
Summary

Resonic Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212502
510(k) Type
Traditional
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2021
Days to Decision
88 days
Submission Type
Summary