# Continental X-Ray Corp.

- Location (FDA's records): Broadview, IL
- FDA decisions: 27 (1988–1997): 27 510(k) clearances
- Product codes: IZO (5), JAA (4), IZZ (3), IXQ (2), IZH (2), KXJ (2), KPR (2), IZF (2), IYB (1), IZI (1), IXL (1), IXR (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
- K972442: Ceiling Mounted Lateral Positioner, Model NO. 6896.002 (Sep 11, 1997)
- K962140: Ict-2000, Integrated C-Arm/Table Multipurpose Radiographic/Fluoroscopic Positioning System Model NO. 6896.300 (Jul 25, 1996)
- K961690: Cardioarc Series: Positioner C-Arm Models NO. 6896.001 and 6896.105 (Jun 27, 1996)
- K954581: Arc Series (Dec 21, 1995)
- K950571: Linear FR Tomographic System: 0MT 8000, Model NO. 6681.270 (Mar 31, 1995)
- K942175: Linear Tomographic System: PMT 6000 (Aug 17, 1994)
- K942100: Model TM EP High Voltage Generator (Jun 7, 1994)
- K934686: Molybdenum/Rhodium Filters (May 26, 1994)

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