FDA 510(k) Applications Submitted by NG POY SIN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K970115 |
01/13/1997 |
POWDER FREE LATEX EXAMINATION GLOVES |
PT MBF BUANA MULTICORPORA |
| K031020 |
03/31/2003 |
FLEXISKIN LATEX EXAMINATION GLOVES, POWDERED, NON STERILE |
PT. MANDIRI INTI BUANA |
| K022343 |
07/19/2002 |
GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, NON STERILE (PROTEIN CONTENT LABELING CLAIM 50UG/G OR LESS) |
PT. WRP BUANA MULTICORPORA |
| K030273 |
01/27/2003 |
GLOVETEX LATEX EXAMINATION GLOVES, POWDERED, BLUE, NON STERILE |
PT. WRP BUANA MULTICORPORA |
| K031754 |
03/31/2003 |
FLEXISKIN POWDER FREE LATEX EXAMINATION GLOVES, NON STERILE |
PT. MANDIRI INTI BUANA |
| K032007 |
06/30/2003 |
GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, BLUE, NON-STERILE CONTAINS 50 MCGIN OR LESS OF TOTAL WATER EXTRACTABLE PR |
PT. WRP BUANA MULTICORPORA |
| K032010 |
06/30/2003 |
GLOVETEX POWDER FREE NITRILE EXAMINATION GLOVES, BLUE, NON-STERILE |
PT. WRP BUANA MULTICORPORA |
| K032011 |
06/30/2003 |
GLOVETEX POWDER FREE WHITE NITRILE EXAMINATION GLOVES, NON-STERILE |
PT. WRP BUANA MULTICORPORA |
| K994426 |
12/30/1999 |
GLOVETEX, LATEX EXAMINATION GLOVES, POWDERED NON-STERILE.(PROTEIN CONTENT LABELING) |
PT. WRP BUANA MULTICORPORA |
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