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HydroCision TenJet Device

Page Type
Cleared 510(K)
510(k) Number
K190804
510(k) Type
Traditional
Applicant
HydroCision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2019
Days to Decision
68 days
Submission Type
Summary

HydroCision TenJet Device

Page Type
Cleared 510(K)
510(k) Number
K190804
510(k) Type
Traditional
Applicant
HydroCision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2019
Days to Decision
68 days
Submission Type
Summary