FDA 510(k) Applications Submitted by K.C. CHOONG
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K990695 |
03/03/1999 |
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED WHITE |
OMNIGRACE (THAILAND) LTD. |
K990696 |
03/03/1999 |
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE,WHITE |
OMNIGRACE (THAILAND) LTD. |
K990698 |
03/03/1999 |
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED PURPLE |
OMNIGRACE (THAILAND) LTD. |
K990701 |
03/03/1999 |
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE, PURPLE |
OMNIGRACE (THAILAND) LTD. |
K990702 |
03/03/1999 |
OMNI GRACE LATEX EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED WITH PROTEIN CLAIM |
OMNIGRACE (THAILAND) LTD. |
K991845 |
05/28/1999 |
PATIENT EXAMINATION GLOVES, NITRILE POWDER FREE, TURQUOISE,NON-STERILE. |
OMNIGRACE LTD. |
K991846 |
05/28/1999 |
PATIENT EXAMINATION GLOVE, NITRILE, POWDERED, TURQUOISE, NON-STERILE |
OMNIGRACE LTD. |
K982716 |
08/04/1998 |
OMNIGRACE LATEX EXAMINATION GLOVE, POWDER-FREE, WITH PROTEIN CLAIM |
OMNIGRACE (THAILAND) LTD. |
K993479 |
10/14/1999 |
OMNI GRACE LATEX EXAMINATION GLOVE, POWDERED, WITH PROTEIN CLAIM (100 MICROGRAMS OR LESS) |
OMNIGRACE (THAILAND) LTD. |
K983725 |
10/22/1998 |
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED, BLUE |
OMNIGRACE LTD. |
K983730 |
10/22/1998 |
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE, BLUE |
OMNIGRACE LTD. |
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