Ansell Healthcare Products, Inc.
Ansell Healthcare Products, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2011.
Top product codes for Ansell Healthcare Products, Inc.
Recent clearances by Ansell Healthcare Products, Inc.
- K111139 — DERMA PRENE ISOTOUCH GREEN STERILE POWDER-FREE POLYISOPRENE SURGICAL GOVES, TESTED FOR U
- K082457 — MICRO-TOUCH NITRATEX STERILE NITRILE POWDER-FREE BLUE EXAMINATION GLOVES (CHEMOTHERAPY USE)
- K042817 — MICRO-TOUCH SMOOTH NITRILE POWDER-FREE BLUE EXAMINATION GLOVES (CHEMOTHERAPY USE)
- K023153 — MICRO-TOUCH NEXT STEP POWDER FREE MEDICAL EXAMINATION GLOVES WITH ALOE AND GLYCEROL
- K013603 — MODIFICATION TO:MICRO TOUCH (R) POWDER FREE LATEX SURGICAL GLOVES , MODEL STYLE 65
- K013604 — MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOVES
- K011593 — MICRO-TOUCH NITRILE POWDER FREE SYNTHETIC MEDICAL EXAMINATION GLOVES, COLOR BLUE NON-STERILE
- K010961 — X-TENDA CUFF POWDER FREE NON-STERILE LATEX EXAMINATION GLOVE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
- K003771 — ENCORE POWDER-FREE LATEX SURGICAL GLOVES, ORTHOPAEDIC WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
- K003769 — ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87
Data sourced from openFDA. This site is unofficial and independent of the FDA.