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Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K200331
510(k) Type
Special
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2020
Days to Decision
29 days
Submission Type
Summary

Rapid Acoustic Pulse Device

Page Type
Cleared 510(K)
510(k) Number
K200331
510(k) Type
Special
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2020
Days to Decision
29 days
Submission Type
Summary