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Soliton Acoustic Wave Device

Page Type
Cleared 510(K)
510(k) Number
K190542
510(k) Type
Traditional
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2019
Days to Decision
81 days
Submission Type
Summary

Soliton Acoustic Wave Device

Page Type
Cleared 510(K)
510(k) Number
K190542
510(k) Type
Traditional
Applicant
Soliton Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2019
Days to Decision
81 days
Submission Type
Summary