Hovik Corp.
Country not established
- Devices
- 1
What Hovik Corp. makes
Hovik Corp. manufactures Holter ECG recorders, which are portable devices used for continuous ambulatory electrocardiographic monitoring to detect cardiac arrhythmias over extended periods.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The portfolio is based in the United States.
Catalogue
Recorder, Holter Electrocardiogram Ref K781843
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hovik Corp. have in the registry?
The registry currently lists 1 device for Hovik Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hovik Corp.'s devices?
Among its 1 most recently registered device, Hovik Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Hovik Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hovik Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hovik Corp. in the registry?
The most recently registered devices listed for Hovik Corp. include RECORDER, HOLTER ELECTROCARDIOGRAM.