# Mega Electronics, Ltd.

- Location (FDA's records): The Hague, NL
- FDA decisions: 4 (1997–2015): 4 510(k) clearances
- Product codes: DXH (2), HCC (1), HIR (1)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Hollister, Inc.: 5 (https://510kreport.com/company/hollister)
- Universal Medical, Inc.: 1 (https://510kreport.com/company/universal-medical)
- Card Guard Scientific Survival, Ltd.: 1 (https://510kreport.com/company/card-guard-scientific-survival)
- Thought Technology, Ltd.: 1 (https://510kreport.com/company/thought-technology)
- Verimed Holdings, Inc.: 1 (https://510kreport.com/company/verimed-holdings)
- Noraxon USA, Inc.: 1 (https://510kreport.com/company/noraxon-usa)

## Firms that cite its devices most
- RhythMedix, LLC: 1 (https://510kreport.com/company/rhythmedix)
- Nanowear, Inc.: 1 (https://510kreport.com/company/nanowear)

## Its most-cited devices
- K131699: Emotion Ecg Mobile (2013), cited by 2
- K143032: eMotion Faros ECG Mobile (2015), cited by 1

## Recent decisions
- K143032: eMotion Faros ECG Mobile (Mar 29, 2015)
- K131699: Emotion Ecg Mobile (Nov 26, 2013)
- K993411: Femiscan Clinic System, Model FS-Ictra and Femiscan Personal System, Model FS-HMTR (Jan 10, 2000)
- K963202: Mega ME 3000 Professional Muscle Tester (May 19, 1997)

Source page: https://510kreport.com/company/mega-electronics