Holta-Med
Country not established
- Devices
- 2
What Holta-Med makes
Holta-Med manufactures cardiac event recorders, including the Holta-Med Recorder for remote patient monitoring of arrhythmias, and the Holta-Med Informer Playback system for reviewing stored cardiac data.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Holta-Med operates from the United States.
Catalogue
Holta-Med Recorder Ref K832395
Regimes: 510(k) Registry: 510(k)Holta-Med Informer Playback Ref K832354
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Holta-Med have in the registry?
The registry currently lists 2 devices for Holta-Med. Devices recorded under merged duplicate company entries are counted once.
Which registries list Holta-Med's devices?
Among its 2 most recently registered devices, Holta-Med has devices listed in FDA 510(k) (2 devices).
What risk classes do Holta-Med's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Holta-Med's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Holta-Med in the registry?
The most recently registered devices listed for Holta-Med include HOLTA-MED RECORDER and HOLTA-MED INFORMER PLAYBACK.