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DUREX LUBRAGEL LATEX CONDOM

Page Type
Cleared 510(K)
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)
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