# Cgr Medical Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 20 (1978–1984): 20 510(k) clearances
- Product codes: IYO (4), JAA (3), JAK (2), IZO (2), IZP (1), IZI (1), IYE (1), ITY (1), IXR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Southeastern Radiation Products, Inc.: 1 (https://510kreport.com/company/southeastern-radiation-products)
- Biospace Med: 1 (https://510kreport.com/company/biospace-med)

## Its most-cited devices
- K833941: ORION (1983), cited by 1
- K843926: Prestilix 1690 (1984), cited by 1

## Recent decisions
- K843926: Prestilix 1690 (Dec 17, 1984)
- K843235: Stenoscop (Nov 8, 1984)
- K843985: Suspension 7 (Nov 5, 1984)
- K841649: Maximax - 4 (Jun 5, 1984)
- K833223: Sonel 3000A (May 9, 1984)
- K833941: ORION (Dec 29, 1983)
- K834306: Phasix-High Frequency Generator (Dec 29, 1983)
- K833846: Process 100 ST (Dec 16, 1983)

Source page: https://510kreport.com/company/cgr-medical