Physiosonics, Inc.
Country not established
- Devices
- 1
What Physiosonics, Inc. makes
Physiosonics, Inc. manufactures the PRESTO 1000 SYSTEM, a medical device designed for therapeutic ultrasound applications in physical rehabilitation and musculoskeletal treatments.
The PRESTO 1000 SYSTEM 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
Presto 1000 System Ref K123565
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physiosonics, Inc. have in the registry?
The registry currently lists 1 device for Physiosonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physiosonics, Inc.'s devices?
Among its 1 most recently registered device, Physiosonics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Physiosonics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Physiosonics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physiosonics, Inc. in the registry?
The most recently registered devices listed for Physiosonics, Inc. include PRESTO 1000 SYSTEM.