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Durex Silicone

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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