American Health Tech., Inc.
Country not established
- Devices
- 1
What American Health Tech., Inc. makes
American Health Tech., Inc. manufactures the SENATEK, a Class I medical device designed for [specific function not provided in data]. The product is intended for [purpose not specified in data], adhering to regulatory standards for low-risk devices.
The SENATEK 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
Senatek Ref K822993
510(k) 510(k)
Frequently asked questions
How many devices does American Health Tech., Inc. have in the registry?
The registry currently lists 1 device for American Health Tech., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Health Tech., Inc.'s devices?
Among its 1 most recently registered device, American Health Tech., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do American Health Tech., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Health Tech., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Health Tech., Inc. in the registry?
The most recently registered devices listed for American Health Tech., Inc. include SENATEK.