Mays and Associates, Inc.
Country not established
- Devices
- 1
What Mays and Associates, Inc. makes
Mays and Associates, Inc. manufactures the OMNIPRO System, a medical device designed for peritoneal dialysis therapy. This system includes components for automated or manual peritoneal dialysis, enabling fluid exchange in the peritoneal cavity to manage chronic kidney disease.
The OMNIPRO System is classified as a Class II device under FDA regulations and has been cleared via the 510(k) pathway. The company is based in the United States.
Catalogue
Omnipro System Ref K050143
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mays and Associates, Inc. have in the registry?
The registry currently lists 1 device for Mays and Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mays and Associates, Inc.'s devices?
Among its 1 most recently registered device, Mays and Associates, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mays and Associates, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mays and Associates, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mays and Associates, Inc. in the registry?
The most recently registered devices listed for Mays and Associates, Inc. include OMNIPRO SYSTEM.