Sensititre Alamar
Country not established
- Devices
- 1
What Sensititre Alamar makes
Sensititre Alamar produces antimicrobial susceptibility testing plates designed for automated detection of bacterial resistance patterns within 18 hours, enabling rapid identification of effective treatments in clinical microbiology settings.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance pathway. The portfolio is regulated in the United States.
Catalogue
Sensititre 18 Hour Susceptibility Plates Ref K962867
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensititre Alamar have in the registry?
The registry currently lists 1 device for Sensititre Alamar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensititre Alamar's devices?
Among its 1 most recently registered device, Sensititre Alamar has devices listed in FDA 510(k) (1 device).
What risk classes do Sensititre Alamar's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sensititre Alamar's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sensititre Alamar in the registry?
The most recently registered devices listed for Sensititre Alamar include SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES.