Mathews Assoc., Inc.
Country not established
- Devices
- 1
What Mathews Assoc., Inc. makes
Mathews Assoc., Inc. manufactures the P.A.T. System, a medical device designed for patient assessment and monitoring in clinical settings.
The P.A.T. System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
P.A.T. System Ref K943035
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mathews Assoc., Inc. have in the registry?
The registry currently lists 1 device for Mathews Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mathews Assoc., Inc.'s devices?
Among its 1 most recently registered device, Mathews Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mathews Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mathews Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mathews Assoc., Inc. in the registry?
The most recently registered devices listed for Mathews Assoc., Inc. include P.A.T. SYSTEM.