Last synced on 14 November 2025 at 11:06 pm

DynaFlex

Page Type
Cleared 510(K)
510(k) Number
K190583
510(k) Type
Traditional
Applicant
DynaFlex
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2019
Days to Decision
113 days
Submission Type
Summary

DynaFlex

Page Type
Cleared 510(K)
510(k) Number
K190583
510(k) Type
Traditional
Applicant
DynaFlex
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2019
Days to Decision
113 days
Submission Type
Summary