Coleman Laboratories
Country not established
- Devices
- 2
What Coleman Laboratories makes
Coleman Laboratories manufactures fluid level monitoring devices designed to track and alert on liquid levels in medical or industrial systems, ensuring operational safety and efficiency.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Triglycerides Determination Ref K802256
Regimes: 510(k) Registry: 510(k)Fluid Level Monitor Ref K133870
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coleman Laboratories have in the registry?
The registry currently lists 2 devices for Coleman Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coleman Laboratories's devices?
Among its 2 most recently registered devices, Coleman Laboratories has devices listed in FDA 510(k) (2 devices).
What risk classes do Coleman Laboratories's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Coleman Laboratories's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coleman Laboratories in the registry?
The most recently registered devices listed for Coleman Laboratories include TRIGLYCERIDES DETERMINATION and FLUID LEVEL MONITOR.