Powell, Goldstein, Frazer & Murphy
Country not established
- Devices
- 1
What Powell, Goldstein, Frazer & Murphy makes
Powell, Goldstein, Frazer & Murphy manufactures the A-V Impulse System Model 6060, a medical device designed for pacing or stimulation of cardiac conduction pathways, likely intended for treating arrhythmias or conduction disorders.
The device falls under FDA Class II regulation and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
A-V Impulse System Model 6060 Ref K964425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Powell, Goldstein, Frazer & Murphy have in the registry?
The registry currently lists 1 device for Powell, Goldstein, Frazer & Murphy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Powell, Goldstein, Frazer & Murphy's devices?
Among its 1 most recently registered device, Powell, Goldstein, Frazer & Murphy has devices listed in FDA 510(k) (1 device).
What risk classes do Powell, Goldstein, Frazer & Murphy's devices fall under?
Among its 1 most recently registered device, the classes recorded for Powell, Goldstein, Frazer & Murphy's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Powell, Goldstein, Frazer & Murphy in the registry?
The most recently registered devices listed for Powell, Goldstein, Frazer & Murphy include A-V IMPULSE SYSTEM MODEL 6060.