Kelley Development Corp.
Country not established
- Devices
- 1
What Kelley Development Corp. makes
Kelley Development Corp. manufactures the ULTRASYSTEM LINSCAN PROBE, a linear array ultrasound scanning probe designed for diagnostic imaging applications.
The ULTRASYSTEM LINSCAN PROBE is classified as a Class II medical device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.
Catalogue
Ultrasystem Linscan Probe Ref K842811
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kelley Development Corp. have in the registry?
The registry currently lists 1 device for Kelley Development Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kelley Development Corp.'s devices?
Among its 1 most recently registered device, Kelley Development Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Kelley Development Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kelley Development Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kelley Development Corp. in the registry?
The most recently registered devices listed for Kelley Development Corp. include ULTRASYSTEM LINSCAN PROBE.