Clifford M. Terry, M.C.
Country not established
- Devices
- 1
What Clifford M. Terry, M.C. makes
Clifford M. Terry, M.C. manufactures the Terry Keratometer, a device used to measure corneal curvature for ophthalmic assessments.
The Terry Keratometer is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Terry Keratometer Ref K781650
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clifford M. Terry, M.C. have in the registry?
The registry currently lists 1 device for Clifford M. Terry, M.C.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clifford M. Terry, M.C.'s devices?
Among its 1 most recently registered device, Clifford M. Terry, M.C. has devices listed in FDA 510(k) (1 device).
What risk classes do Clifford M. Terry, M.C.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Clifford M. Terry, M.C.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Clifford M. Terry, M.C. in the registry?
The most recently registered devices listed for Clifford M. Terry, M.C. include TERRY KERATOMETER.