# Resonex, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 21 (1988–1994): 21 510(k) clearances
- Product codes: LNH (21)
- 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
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Biosound, Inc.: 1 (https://510kreport.com/company/biosound)

## Its most-cited devices
- K924154: Kinematic Mri Moviemaker (1992), cited by 2

## Recent decisions
- K935369: Fast Spin Echo (Fse) (Mar 21, 1994)
- K935570: Noise Filter for Paradigm Magnetic Resonance Imaging System (Mar 16, 1994)
- K931392: Ecg Gating Unit (Nov 2, 1993)
- K923870: 3DTOF Mra (Jan 12, 1993)
- K924154: Kinematic Mri Moviemaker (Nov 23, 1992)
- K923823: 3D Imaging (Oct 30, 1992)
- K922677: Magnetization Transfer Contrast (Sep 4, 1992)
- K920254: Coils for RX4000 & RX5000 Mri Systems (Jun 22, 1992)

Source page: https://510kreport.com/company/resonex