Syracuse Research Corp.
Country not established
- Devices
- 1
What Syracuse Research Corp. makes
Syracuse Research Corp. manufactures CINEMEASURE™, a device used for quantitative analysis of cardiac motion and function from cinefluoroscopic images, primarily for assessing left ventricular performance in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with CINEMEASURE™ authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Cinemeasure (Tm) Ref K910654
510(k) 510(k)
Frequently asked questions
How many devices does Syracuse Research Corp. have in the registry?
The registry currently lists 1 device for Syracuse Research Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syracuse Research Corp.'s devices?
Among its 1 most recently registered device, Syracuse Research Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Syracuse Research Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Syracuse Research Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syracuse Research Corp. in the registry?
The most recently registered devices listed for Syracuse Research Corp. include CINEMEASURE (TM).