Last synced on 14 November 2025 at 11:06 pm

Durex Silicone

Page Type
Cleared 510(K)
510(k) Number
K143532
510(k) Type
Traditional
Applicant
Reckitt Benckiser LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
231 days
Submission Type
Summary

Durex Silicone

Page Type
Cleared 510(K)
510(k) Number
K143532
510(k) Type
Traditional
Applicant
Reckitt Benckiser LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
231 days
Submission Type
Summary