FDA 510(k) Applications Submitted by OMNIGRACE LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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. |
| 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. |
| K973134 |
08/21/1997 |
OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED |
OMNIGRACE LTD. |
| K993050 |
09/10/1999 |
OMNI GRACE NITRILE, GREEN, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED |
OMNIGRACE LTD. |
| K993419 |
10/12/1999 |
OMNIGRACE LATEX EXAMINATION GLOVE, POWDER-FREE; POLYMER COATED WITH PROTEIN CLAIM (50 MICROGRAMS OR LESS) |
OMNIGRACE LTD. |
| K994246 |
12/16/1999 |
OMNI GRACE NITRILE, BLUE, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED |
OMNIGRACE LTD. |
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