Compass Medical Technologies, Inc.
Country not established
- Devices
- 1
What Compass Medical Technologies, Inc. makes
Compass Medical Technologies, Inc. manufactures the RT2, a device used for assessing rigidity and tumescence in medical evaluations, likely for penile function testing.
The RT2 is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
RT2 Rigidity And Tumescence Test Ref K925931
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Compass Medical Technologies, Inc. have in the registry?
The registry currently lists 1 device for Compass Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Compass Medical Technologies, Inc.'s devices?
Among its 1 most recently registered device, Compass Medical Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Compass Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Compass Medical Technologies, Inc. include RT2 RIGIDITY AND TUMESCENCE TEST.