Montifore Medical Center
Country not established
- Devices
- 1
What Montifore Medical Center makes
Montifore Medical Center manufactures the L-LINEX-RAY FLUORESCENCE device, a system designed for radiographic imaging using fluorescence technology.
This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company operates in the United States.
Catalogue
L-Linex-Ray Fluorescence Ref K911749
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Montifore Medical Center have in the registry?
The registry currently lists 1 device for Montifore Medical Center. Devices recorded under merged duplicate company entries are counted once.
Which registries list Montifore Medical Center's devices?
Among its 1 most recently registered device, Montifore Medical Center has devices listed in FDA 510(k) (1 device).
What risk classes do Montifore Medical Center's devices fall under?
Among its 1 most recently registered device, the classes recorded for Montifore Medical Center's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Montifore Medical Center in the registry?
The most recently registered devices listed for Montifore Medical Center include L-LINEX-RAY FLUORESCENCE.