# Magnetic Resonance Equipment Corp.

- Location (FDA's records): Bay Shore, NY
- FDA decisions: 5 (1993–2001): 5 510(k) clearances
- Product codes: DQA (2), CCK (2), DSK (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Odam: 1 (https://510kreport.com/company/odam)
- Schiller Medical S.A.: 1 (https://510kreport.com/company/schiller-medical)

## Its most-cited devices
- K954120: Model 9500 MR-Compatible Multigas Monitor (1997), cited by 2

## Recent decisions
- K003982: Temperature Function, Model 9500 Multigas Monitor (Jan 26, 2001)
- K983250: Invasive Blood Pressure (Ibp) Function, Model 9500 Multigas Monitor (Dec 12, 1999)
- K954120: Model 9500 MR-Compatible Multigas Monitor (Apr 2, 1997)
- K924285: Model 3500 MR-Compatible Pulse Oximeter (May 11, 1993)
- K924282: Model 320 MR-Compatible Pulse Oximeter (May 7, 1993)

Source page: https://510kreport.com/company/magnetic-resonance-equipment