# Med-West, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 11 (1983–1988): 11 510(k) clearances
- Product codes: FIQ (2), LFK (2), NAD (1), DXT (1), INO (1), DRE (1), DWF (1), LFJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K880877: Contrast Injection Device (May 31, 1988)
- K880398: Power Toilet Elevator (Mar 17, 1988)
- K874470: Mwi 400 Wound Dressing (Dec 18, 1987)
- K872724: Sheath/Dilators (Sep 15, 1987)
- K854612: Acute Hemodialysis Tray, Cat.#09-9540-7 (Jan 3, 1986)
- K852162: Mni 400 Injection Caps (Jun 12, 1985)
- K842342: Mwi 888 & 666 Double Lumen Subclavian (Jun 14, 1984)
- K832124: CPC, Couble Lumen Cardioplegia-Air Aspi (Aug 12, 1983)

Source page: https://510kreport.com/company/med-west