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Durex Polyisoprene Condom

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241617
510(k) Type
Traditional
Applicant
RB Health (US) LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
268 days
Submission Type
Statement

Durex Polyisoprene Condom

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241617
510(k) Type
Traditional
Applicant
RB Health (US) LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
268 days
Submission Type
Statement