Clinical Microsystems Intl.
Country not established
- Devices
- 2
What Clinical Microsystems Intl. makes
Clinical Microsystems Intl. manufactures the RESPONDER II, a device for monitoring and recording cardiac electrical activity, and the MULTIVARIATE DIGITAL CARDIOGRAPH, which captures and digitizes multiple cardiac signals for diagnostic analysis.
These products fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Responder Ii Ref K801894
Regimes: 510(k) Registry: 510(k)Multivariate Digital Cardiograph Ref K840875
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical Microsystems Intl. have in the registry?
The registry currently lists 2 devices for Clinical Microsystems Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Microsystems Intl.'s devices?
Among its 2 most recently registered devices, Clinical Microsystems Intl. has devices listed in FDA 510(k) (2 devices).
What risk classes do Clinical Microsystems Intl.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clinical Microsystems Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Microsystems Intl. in the registry?
The most recently registered devices listed for Clinical Microsystems Intl. include RESPONDER II and MULTIVARIATE DIGITAL CARDIOGRAPH.