FDA 510(k) Applications Submitted by KATHLEEN J HARRIS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K050184 |
01/27/2005 |
BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K050533 |
03/02/2005 |
ECLIPSE LATEX POWDER FREE STERILE SURGEON'S GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K050899 |
04/11/2005 |
BIOGEL LATEX STERILE POWDER-FREE GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K032124 |
07/10/2003 |
DUREX PLAY LUBRICANT |
SSL AMERICAS, INC. |
| K032227 |
07/21/2003 |
DUREX FLAVORED LATEX CONDOM |
SSL AMERICAS, INC. |
| K053102 |
11/04/2005 |
BIOGEL SKINSENSE POWDER-FREE NON-LATEX SURGEON'S GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K053441 |
12/09/2005 |
BIOGEL LATEX POWDER FREE STERILE SURGEON'S GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K053442 |
12/09/2005 |
BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K053443 |
12/09/2005 |
BIOGEL ECLIPSE NON-PYROGENIC LATEX POWDER-FREE STERILE SURGEON'S GLOVE |
REGENT MEDICAL AMERICAS, LLC |
| K040185 |
01/27/2004 |
DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM |
SSL AMERICAS |
| K040353 |
02/12/2004 |
FLIGHT SOCK |
SSL AMERICAS, INC. |
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