Ralph Lindel, D.C.
Country not established
- Devices
- 1
What Ralph Lindel, D.C. makes
The company produces the X-Ray Assist Bar, a device designed to support and stabilize patients during radiographic imaging procedures, ensuring proper positioning and alignment for accurate X-ray imaging.
This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.
Catalogue
X-Ray Assist Bar Ref K972000
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ralph Lindel, D.C. have in the registry?
The registry currently lists 1 device for Ralph Lindel, D.C.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ralph Lindel, D.C.'s devices?
Among its 1 most recently registered device, Ralph Lindel, D.C. has devices listed in FDA 510(k) (1 device).
What risk classes do Ralph Lindel, D.C.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ralph Lindel, D.C.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ralph Lindel, D.C. in the registry?
The most recently registered devices listed for Ralph Lindel, D.C. include X-RAY ASSIST BAR.