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Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K201801
510(k) Type
Traditional
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2021
Days to Decision
213 days
Submission Type
Summary

Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K201801
510(k) Type
Traditional
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2021
Days to Decision
213 days
Submission Type
Summary