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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