Chek-Med Systems
Country not established
- Devices
- 3
What Chek-Med Systems makes
Chek-Med Systems manufactures endoscopic markers and imaging wands, including the Spot Endoscopic Marker and Polar Wand, designed for precise tissue identification and procedural guidance during endoscopic procedures.
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
Polar Wand Ref K041783
Regimes: 510(k) Registry: 510(k)Spot Endoscopic Marker Ref K993951
Regimes: 510(k) Registry: 510(k)Polar Wand Ref K021387
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chek-Med Systems have in the registry?
The registry currently lists 3 devices for Chek-Med Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chek-Med Systems's devices?
Among its 3 most recently registered devices, Chek-Med Systems has devices listed in FDA 510(k) (3 devices).
What risk classes do Chek-Med Systems's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Chek-Med Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chek-Med Systems in the registry?
The most recently registered devices listed for Chek-Med Systems include POLAR WAND and SPOT ENDOSCOPIC MARKER.