# Medic, Inc.

- Location (FDA's records): Fremont, NE
- FDA decisions: 12 (1993–2002): 12 510(k) clearances
- Product codes: LNH (11), MOS (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 5 (1 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
- Resonance Innovations, LLC: 4 (https://510kreport.com/company/resonance-innovations)

## Its most-cited devices
- K951649: Model #801GE1500 Pediatric Array Coil (1995), cited by 3
- K933659: Model #100GE1500 Lower Extrem Quad Detect Array Coil (1993), cited by 1
- K022395: 1.5T Scanmed PV Array (2002), cited by 1

## Recent decisions
- K022395: 1.5T Scanmed PV Array (Aug 13, 2002)
- K951649: Model #801GE1500 Pediatric Array Coil (Jun 22, 1995)
- K942874: Model #300TO3500 Shoulder Coil (Dec 8, 1994)
- K942873: Model #700TO3500 Neck/Abdominal Coil (Dec 2, 1994)
- K942875: Model #900TO3500 Head/Neck Coil (Dec 2, 1994)
- K942355: Model #310T03500 Wrist Coil (Sep 16, 1994)
- K940874: Model 900GE1500 Head/Neck Coil (Jun 3, 1994)
- K933296: Model #310GE1500 Wrist Coil (Mar 17, 1994)

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