Ameritek Research, LLC
Country not established
- Devices
- 1
What Ameritek Research, LLC makes
Ameritek Research, LLC manufactures an in-vitro diagnostic test kit designed to detect vaginitis, enabling rapid clinical assessment of vaginal infections.
The company’s vaginitis test kit is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
In-Vitro Diagnostic Vaginitis Test Kit Ref K050352
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ameritek Research, LLC have in the registry?
The registry currently lists 1 device for Ameritek Research, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ameritek Research, LLC's devices?
Among its 1 most recently registered device, Ameritek Research, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Ameritek Research, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ameritek Research, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ameritek Research, LLC in the registry?
The most recently registered devices listed for Ameritek Research, LLC include IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT.