Keith E. Abbott
Country not established
- Devices
- 1
What Keith E. Abbott makes
Keith E. Abbott manufactures an antibody to native deoxyribonuclease kit, designed for diagnostic use in detecting deoxyribonuclease activity in clinical samples.
The product is classified as Class II under FDA regulations and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Antibody To Native Deoxyribonuclease Kit Ref K791928
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keith E. Abbott have in the registry?
The registry currently lists 1 device for Keith E. Abbott. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keith E. Abbott's devices?
Among its 1 most recently registered device, Keith E. Abbott has devices listed in FDA 510(k) (1 device).
What risk classes do Keith E. Abbott's devices fall under?
Among its 1 most recently registered device, the classes recorded for Keith E. Abbott's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Keith E. Abbott in the registry?
The most recently registered devices listed for Keith E. Abbott include ANTIBODY TO NATIVE DEOXYRIBONUCLEASE KIT.