Electro-Cap Intl., Inc.
Country not established FDA establishment FEI 1000119368
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Electro-Cap Intl., Inc. makes
Electro-Cap Intl., Inc. manufactures electro-gel, electrode caps, and the Electro-Cap system for use in electroencephalography.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Electro-Gel Ref K111717
510(k) 510(k)Electro-Cap System Ref K112319
510(k) 510(k)Electrode Cap Ref K780045
510(k) 510(k)
Company details
- FDA FEI number
- 1000119368
- Address
- 1011 W Lexington Rd, EATON, OH, 45320
Frequently asked questions
How many devices does ELECTRO-CAP INTL., INC. have in the registry?
The registry currently lists 3 devices for ELECTRO-CAP INTL., INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ELECTRO-CAP INTL., INC.'s devices?
Among its 3 most recently registered devices, ELECTRO-CAP INTL., INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do ELECTRO-CAP INTL., INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for ELECTRO-CAP INTL., INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ELECTRO-CAP INTL., INC. in the registry?
The most recently registered devices listed for ELECTRO-CAP INTL., INC. include ELECTRO-GEL, ELECTRO-CAP SYSTEM and ELECTRODE CAP.