Paraproducts, Inc.
Country not established
- Devices
- 1
What Paraproducts, Inc. makes
Paraproducts, Inc. manufactures the POSITUBE, a device designed for tracheostomy care and airway management, including cuffed tracheostomy tubes and related accessories.
The POSITUBE falls under FDA Class II regulation and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Positube Ref K000045
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paraproducts, Inc. have in the registry?
The registry currently lists 1 device for Paraproducts, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paraproducts, Inc.'s devices?
Among its 1 most recently registered device, Paraproducts, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Paraproducts, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Paraproducts, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Paraproducts, Inc. in the registry?
The most recently registered devices listed for Paraproducts, Inc. include POSITUBE.