FDA 510(k) Applications Submitted by SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K052030 |
07/27/2005 |
SURGEON'S GLOVE, POWDER FREE |
SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD. |
K060229 |
01/30/2006 |
POWDER-FREE BLACK LATEX EXAMINATION GLOVES WITH PROTEIN LABELING (50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PROTE |
SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD. |
K040406 |
02/17/2004 |
POLYMER COATED, CHLORINATED, POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING (LESS THAN 50 UG/G PER GLOVE) |
SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD. |
K040408 |
02/17/2004 |
POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING (LESS THAN 50 UG/G PER GLOVE) |
SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD. |
K052031 |
07/27/2005 |
POWDERED LATEX SURGEON'S GLOVE |
SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD. |
K092617 |
08/26/2009 |
ROYAL GUARD |
SHUN THAI RUBBER GLOVES INDUSTRY PUBLIC CO., LTD. |
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