# Contour Medical Technology, Inc.

- Location (FDA's records): Lavergne, TN
- FDA decisions: 9 (1996–1997): 9 510(k) clearances
- Product codes: FMT (6), MKJ (2), DRX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Cardiac Science Corporation: 1 (https://510kreport.com/company/cardiac-science)

## Its most-cited devices
- K960329: Disposable Hydrogel Defibrillation Electrode/Pad (1996), cited by 1

## Recent decisions
- K970391: Quantum Edge Pediatric Defirbrillation Electrodes (Mar 6, 1997)
- K970125: Noah Monitoring Electrode System (Mar 4, 1997)
- K960329: Disposable Hydrogel Defibrillation Electrode/Pad (Jul 2, 1996)
- K952804: Temperature Probe-TP450 (Apr 4, 1996)
- K952807: Temperature Probe-TP650 (Apr 4, 1996)
- K952805: Temperature Probe-TP550 (Apr 4, 1996)
- K952801: Temperature Probe-TP250 (Apr 4, 1996)
- K952803: Temperature Probe-TP350 (Apr 4, 1996)

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