Agram Export-Import Co.
Country not established
- Devices
- 1
What Agram Export-Import Co. makes
Agram Export-Import Co. manufactures the Agram Spiral Electrode, a device designed for cardiac ablation procedures to treat arrhythmias by creating precise lesions in heart tissue.
The company’s portfolio is regulated under FDA’s Class II designation and requires 510(k) clearance. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Agram Spyral Electrode Ref K934779
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Agram Export-Import Co. have in the registry?
The registry currently lists 1 device for Agram Export-Import Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Agram Export-Import Co.'s devices?
Among its 1 most recently registered device, Agram Export-Import Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Agram Export-Import Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Agram Export-Import Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Agram Export-Import Co. in the registry?
The most recently registered devices listed for Agram Export-Import Co. include AGRAM SPYRAL ELECTRODE.