Tes Electrical Electronic Corp.
ChinaFDA applicant, unverified
- Devices
- 1
What Tes Electrical Electronic Corp. makes
Tes Electrical Electronic Corp. manufactures the TES-20, a medical device designed for electrophysiological monitoring and cardiac rhythm analysis, including pacemaker and defibrillator diagnostics.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Tes-20 Ref K992425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tes Electrical Electronic Corp. have in the registry?
The registry currently lists 1 device for Tes Electrical Electronic Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tes Electrical Electronic Corp.'s devices?
Among its 1 most recently registered device, Tes Electrical Electronic Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Tes Electrical Electronic Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tes Electrical Electronic Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tes Electrical Electronic Corp. in the registry?
The most recently registered devices listed for Tes Electrical Electronic Corp. include TES-20.