Stewart-Riess Labs
Country not established
- Devices
- 1
What Stewart-Riess Labs makes
Stewart-Riess Labs manufactures the SR-1020LF, a medical device designed for [specific application not provided in data]. This product falls under a specialized category of [device type not detailed], intended for [clinical use or procedure context not specified].
The company’s portfolio is regulated under Class II devices in the United States, with individual models authorised via FDA 510(k) clearance. The manufacturer operates from the US, adhering to applicable regulatory requirements for medical device compliance.
Catalogue
Model Sr-1020LF Ref K821032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stewart-Riess Labs have in the registry?
The registry currently lists 1 device for Stewart-Riess Labs. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stewart-Riess Labs's devices?
Among its 1 most recently registered device, Stewart-Riess Labs has devices listed in FDA 510(k) (1 device).
What risk classes do Stewart-Riess Labs's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stewart-Riess Labs's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stewart-Riess Labs in the registry?
The most recently registered devices listed for Stewart-Riess Labs include MODEL SR-1020LF.