Electronic Monitors, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Electronic Monitors, Inc. makes
Electronic Monitors, Inc. manufactures the RE1000 Heart Rate Monitor, a device for continuous cardiac monitoring, along with the LIFE-MASK Infant Resuscitator, a manual ventilation tool for neonatal resuscitation, and EMITENS Electrodes, reusable adhesive electrodes for electrocardiogram (ECG) applications.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are registered in the United States, where the manufacturer is based.
Catalogue
RE1000 Heart Rate Monitor Ref K822319
Regimes: 510(k) Registry: 510(k)Life-Mask Infant Resuscitator Ref K842696
Regimes: 510(k) Registry: 510(k)Emitens Electrodes Ref K922393
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electronic Monitors, Inc. have in the registry?
The registry currently lists 3 devices for Electronic Monitors, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electronic Monitors, Inc.'s devices?
Among its 3 most recently registered devices, Electronic Monitors, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Electronic Monitors, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Electronic Monitors, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electronic Monitors, Inc. in the registry?
The most recently registered devices listed for Electronic Monitors, Inc. include RE1000 HEART RATE MONITOR, LIFE-MASK INFANT RESUSCITATOR and EMITENS ELECTRODES.