Contour Medical Systems, Inc.
Country not established
- Devices
- 1
What Contour Medical Systems, Inc. makes
Contour Medical Systems, Inc. manufactures the CEMAX-1000, a Class I medical device designed for electrocardiogram (ECG) monitoring and analysis, enabling real-time cardiac rhythm assessment.
The CEMAX-1000 is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Cemax-1000 Ref K833525
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Contour Medical Systems, Inc. have in the registry?
The registry currently lists 1 device for Contour Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Contour Medical Systems, Inc.'s devices?
Among its 1 most recently registered device, Contour Medical Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Contour Medical Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Contour Medical Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Contour Medical Systems, Inc. in the registry?
The most recently registered devices listed for Contour Medical Systems, Inc. include CEMAX-1000.