Med-West, Inc.
Med-West, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1988.
Top product codes for Med-West, Inc.
Recent clearances by Med-West, Inc.
- K880877 — CONTRAST INJECTION DEVICE
- K880398 — POWER TOILET ELEVATOR
- K874470 — MWI 400 WOUND DRESSING
- K872724 — SHEATH/DILATORS
- K854612 — ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7
- K852162 — MNI 400 INJECTION CAPS
- K842342 — MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN
- K832124 — CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI
- K831828 — TEFLON FEMORAL CATHETER MWI 100,10 &
- K831401 — SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS
- K831440 — SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260
Data sourced from openFDA. This site is unofficial and independent of the FDA.