Omnigrace , Ltd.
Omnigrace , Ltd. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2000.
Top product codes for Omnigrace , Ltd.
Recent clearances by Omnigrace , Ltd.
- K994246 — OMNI GRACE NITRILE, BLUE, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED
- K993419 — OMNIGRACE LATEX EXAMINATION GLOVE, POWDER-FREE; POLYMER COATED WITH PROTEIN CLAIM (50 MICROGRAMS OR LESS)
- K993050 — OMNI GRACE NITRILE, GREEN, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED
- K991845 — PATIENT EXAMINATION GLOVES, NITRILE POWDER FREE, TURQUOISE,NON-STERILE.
- K991846 — PATIENT EXAMINATION GLOVE, NITRILE, POWDERED, TURQUOISE, NON-STERILE
- K983730 — OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE, BLUE
- K983725 — OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED, BLUE
- K973134 — OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED
Data sourced from openFDA. This site is unofficial and independent of the FDA.