Mega Electronics, Ltd.
Country not established
- Devices
- 4
What Mega Electronics, Ltd. makes
Mega Electronics, Ltd. manufactures portable and clinic-based cardiac monitoring systems, including the FEMISCAN CLINIC SYSTEM (FS-ICTRA) and FEMISCAN PERSONAL SYSTEM (FS-HMTR) for electrocardiogram (ECG) recording, as well as the eMotion Faros ECG Mobile and EMOTION ECG Mobile for mobile ECG diagnostics. The company also produces the MEGA ME 3000 PROFESSIONAL MUSCLE TESTER, a device for assessing muscle function and strength.
These devices are classified under Class II by the FDA and are listed under the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
eMotion Faros ECG Mobile Ref K143032
Regimes: 510(k) Registry: 510(k)Mega Me 3000 Professional Muscle Tester Ref K963202
Regimes: 510(k) Registry: 510(k)Emotion Ecg Mobile Ref K131699
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mega Electronics, Ltd. have in the registry?
The registry currently lists 4 devices for Mega Electronics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mega Electronics, Ltd.'s devices?
Among its 4 most recently registered devices, Mega Electronics, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Mega Electronics, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mega Electronics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mega Electronics, Ltd. in the registry?
The most recently registered devices listed for Mega Electronics, Ltd. include FEMISCAN CLINIC SYSTEM, MODEL FS-ICTRA AND FEMISCAN PERSONAL SYSTEM, MODEL FS-HMTR, eMotion Faros ECG Mobile, MEGA ME 3000 PROFESSIONAL MUSCLE TESTER and EMOTION ECG MOBILE.