Martin Electric Co.
Country not established
- Devices
- 1
What Martin Electric Co. makes
Martin Electric Co. manufactures the DEBUTRON, a Class I medical electrical device designed for diagnostic or therapeutic use in cardiology, specifically for cardiac pacing or defibrillation testing.
The DEBUTRON is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Debutron Ref K782119
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Martin Electric Co. have in the registry?
The registry currently lists 1 device for Martin Electric Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Martin Electric Co.'s devices?
Among its 1 most recently registered device, Martin Electric Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Martin Electric Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Martin Electric Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Martin Electric Co. in the registry?
The most recently registered devices listed for Martin Electric Co. include DEBUTRON.