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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