FDA 510(k) Applications Submitted by JOYCE NING

FDA 510(k) Number Submission Date Device Name Applicant
K020308 01/29/2002 REGENT BIOGEL SKINSENSE STERILE POWDER-FREE, SYNTHETIC POLYISOPRENE SURGEON'S GLOVE SSL AMERICA'S, INC.
K020659 03/01/2002 DUREX LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT SSL AMERICAS, INC.


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