Physio, Inc.
Country not established
- Devices
- 1
What Physio, Inc. makes
Physio, Inc. manufactures acetate-free dialysate solutions, a sterile fluid used in hemodialysis to remove waste and excess fluids from patients with kidney failure.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Acetate-Free Dialyslate Solution Ref K903835
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physio, Inc. have in the registry?
The registry currently lists 1 device for Physio, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physio, Inc.'s devices?
Among its 1 most recently registered device, Physio, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Physio, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Physio, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physio, Inc. in the registry?
The most recently registered devices listed for Physio, Inc. include ACETATE-FREE DIALYSLATE SOLUTION.