Cefar Medical Products, Inc.
Country not established
- Devices
- 1
What Cefar Medical Products, Inc. makes
Cefar Medical Products, Inc. manufactures the CEFAR DUAL, a medical device designed for diagnostic imaging of the gastrointestinal tract, specifically for dual-contrast studies to enhance visualization of the colon and small intestine.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Cefar Dual Ref K883236
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cefar Medical Products, Inc. have in the registry?
The registry currently lists 1 device for Cefar Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cefar Medical Products, Inc.'s devices?
Among its 1 most recently registered device, Cefar Medical Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cefar Medical Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cefar Medical Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cefar Medical Products, Inc. in the registry?
The most recently registered devices listed for Cefar Medical Products, Inc. include CEFAR DUAL.