# Spectrum X-Ray Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1979–1993): 9 510(k) clearances
- Product codes: IXR (3), KXH (3), IZZ (1), KPX (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
- K933134: Spectrum DG-P7000 Pediatric Cradle (Oct 7, 1993)
- K931563: Spectrum Mark I Special Procedures Table (Aug 23, 1993)
- K870707: Pentamax 1 Model B Table System (May 14, 1987)
- K834494: Spectrum X-Ray Corp (Feb 21, 1984)
- K840463: Digital Cradle (Feb 21, 1984)
- K827450: Simplamatic Iii (May 19, 1982)
- K813561: Spectrum Pediatric Cardle Table (Jan 29, 1982)
- K791812: Spectrum Emergency & Trauma Table System (Nov 5, 1979)

Source page: https://510kreport.com/company/spectrum-x-ray