# Rms Div.

- Location (FDA's records): Addison, IL
- FDA decisions: 10 (1989–1996): 10 510(k) clearances
- Product codes: IXR (2), IXL (2), EJT (1), CCW (1), EIX (1), HTY (1), IZZ (1), EJS (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
- K963367: RMS K-Wire (Oct 30, 1996)
- K954438: Sunmed's Greenline Fiber Optic Laryngoscope (Dec 29, 1995)
- K944848: The Vivacare T.P.S. Probe (Dec 14, 1994)
- K944557: DW250 #91 (Nov 3, 1994)
- K941625: DW234 #29 (Jun 22, 1994)
- K902403: Elite R/F Spot Film Drive (Aug 1, 1990)
- K902146: SFD-035 Spot Film Device (May 31, 1990)
- K896665: Ext-600 Table, Radiographic, Elevating (Jan 22, 1990)

Source page: https://510kreport.com/company/rms-div