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DUREX SYNTHETIC POLYISOPRENE MALE CONDOM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072169
510(k) Type
Abbreviated
Applicant
SSL AMERICAS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2008
Days to Decision
318 days
Submission Type
Summary

DUREX SYNTHETIC POLYISOPRENE MALE CONDOM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072169
510(k) Type
Abbreviated
Applicant
SSL AMERICAS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2008
Days to Decision
318 days
Submission Type
Summary