Davis Assoc.
Country not established
- Devices
- 1
What Davis Assoc. makes
Davis Assoc. manufactures the ACUTRON, a medical device designed for precise measurement and monitoring in clinical settings, likely used in procedures requiring accurate timing or dosage control.
The ACUTRON is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Acutron Ref K880042
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Davis Assoc. have in the registry?
The registry currently lists 1 device for Davis Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Davis Assoc.'s devices?
Among its 1 most recently registered device, Davis Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Davis Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Davis Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Davis Assoc. in the registry?
The most recently registered devices listed for Davis Assoc. include ACUTRON.