American Ergo Systems
Country not established
- Devices
- 1
What American Ergo Systems makes
American Ergo Systems manufactures the ERGO DIAGNOSTIC CARD, a diagnostic tool designed for ergonomic assessments and workplace evaluations.
The ERGO DIAGNOSTIC CARD is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Ergo Diagnostic Card Ref K834145
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Ergo Systems have in the registry?
The registry currently lists 1 device for American Ergo Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Ergo Systems's devices?
Among its 1 most recently registered device, American Ergo Systems has devices listed in FDA 510(k) (1 device).
What risk classes do American Ergo Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for American Ergo Systems's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Ergo Systems in the registry?
The most recently registered devices listed for American Ergo Systems include ERGO DIAGNOSTIC CARD.