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FDA 510(k) Applications Submitted by LONDON INTL. LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980174
01/20/1998
DUREX COLORS AND SCENTS
LONDON INTL. LLC.
K980204
01/20/1998
DUREX LATEX CONDOMS
LONDON INTL. LLC.
K980785
03/02/1998
STERILE, POWDERFREE LATEX EXAMINATION GLOVE
LONDON INTL. LLC.
K982924
08/20/1998
DUREX SENSIDOM LATEX CONDOM
LONDON INTL. LLC.
K983380
09/25/1998
DUREX LUBRAGEL LATEX CONDOM
LONDON INTL. LLC.
K980319
01/27/1998
DUREX ULTRA COMFORT
LONDON INTL. LLC.
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