# Medicor USA, Ltd.

- Location (FDA's records): Columbus, OH
- FDA decisions: 14 (1978–1986): 14 510(k) clearances
- Product codes: IYB (2), IXR (2), FRF (2), KPR (2), LCH (1), BZN (1), JJS (1), BZL (1), JAA (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
- K861994: Model RS-3I Radiographic/Fluroscopic X-Ray System (Jul 18, 1986)
- K861995: Model RS-3 Radiographic Stand (Jun 19, 1986)
- K860025: Model MS-325 Radiographic X-Ray Generator (May 7, 1986)
- K850761: Model PCX/Emy 525A Microprocesssor Control X-Ray C (Sep 19, 1985)
- K851358: Model Bion 2/Type 90 Room Ionizer (Jul 1, 1985)
- K851094: Model Bion 1/Type 1084T Car Ionizer (Jun 19, 1985)
- K843335: Floor Mounted X-Ray Tubestand (Nov 27, 1984)
- K840227: Urolix-3 Urological Table (Mar 23, 1984)

Source page: https://510kreport.com/company/medicor-usa