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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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