Elitech
Country not established
- Devices
- 1
What Elitech makes
Elitech manufactures the MRSA/SA ELITE MGB, a device designed for detecting methicillin-resistant *Staphylococcus aureus* (MRSA) and *Staphylococcus aureus* (SA) in clinical samples.
The MRSA/SA ELITE MGB is classified as a Class II medical device and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Mrsa/SA Elite Mgb Ref K112937
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elitech have in the registry?
The registry currently lists 1 device for Elitech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elitech's devices?
Among its 1 most recently registered device, Elitech has devices listed in FDA 510(k) (1 device).
What risk classes do Elitech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Elitech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elitech in the registry?
The most recently registered devices listed for Elitech include MRSA/SA ELITE MGB.