Last synced on 14 November 2025 at 11:06 pm

IODOFLEX

Page Type
Cleared 510(K)
510(k) Number
K190756
510(k) Type
Traditional
Applicant
Smith & Nephew Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
270 days
Submission Type
Summary

IODOFLEX

Page Type
Cleared 510(K)
510(k) Number
K190756
510(k) Type
Traditional
Applicant
Smith & Nephew Medical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
270 days
Submission Type
Summary