Ventura Medical Electronics
Country not established
- Devices
- 2
What Ventura Medical Electronics makes
Ventura Medical Electronics manufactures the AXION IV Goldline Series and the AXION 5 modification, both of which are external defibrillators designed for emergency cardiac resuscitation. These devices are intended for use in pre-hospital and clinical settings to deliver synchronized and unsynchronized electrical shocks to restore normal heart rhythm in patients experiencing ventricular fibrillation or ventricular tachycardia.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The devices are listed in the FDA’s 510(k) database, adhering to U.S. regulatory requirements for defibrillators. The manufacturer operates from the United States.
Catalogue
Axion Iv Goldline Series Ref K862602
Regimes: 510(k) Registry: 510(k)Axion 5, Modification Ref K911814
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ventura Medical Electronics have in the registry?
The registry currently lists 2 devices for Ventura Medical Electronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ventura Medical Electronics's devices?
Among its 2 most recently registered devices, Ventura Medical Electronics has devices listed in FDA 510(k) (2 devices).
What risk classes do Ventura Medical Electronics's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ventura Medical Electronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ventura Medical Electronics in the registry?
The most recently registered devices listed for Ventura Medical Electronics include AXION IV GOLDLINE SERIES and AXION 5, MODIFICATION.