Last synced on 14 November 2025 at 11:06 pm

Primary Relief

Page Type
Cleared 510(K)
510(k) Number
K221425
510(k) Type
Traditional
Applicant
Dyansys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2022
Days to Decision
120 days
Submission Type
Summary

Primary Relief

Page Type
Cleared 510(K)
510(k) Number
K221425
510(k) Type
Traditional
Applicant
Dyansys, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2022
Days to Decision
120 days
Submission Type
Summary