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DUREX LUBRAGEL LATEX CONDOM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983380
510(k) Type
Abbreviated
Applicant
LONDON INTL. LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1998
Days to Decision
52 days
Submission Type
Summary

DUREX LUBRAGEL LATEX CONDOM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983380
510(k) Type
Abbreviated
Applicant
LONDON INTL. LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1998
Days to Decision
52 days
Submission Type
Summary