Intrumed, Inc.
Country not established
- Devices
- 1
What Intrumed, Inc. makes
Intrumed, Inc. manufactures the INSTRUTAINER, a medical device designed for respiratory therapy and airway clearance, typically used in pediatric and adult patients to assist with mucus removal and lung function improvement.
The INSTRUTAINER is classified as a Class II device under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Instrutainer Ref K844672
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intrumed, Inc. have in the registry?
The registry currently lists 1 device for Intrumed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intrumed, Inc.'s devices?
Among its 1 most recently registered device, Intrumed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intrumed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intrumed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intrumed, Inc. in the registry?
The most recently registered devices listed for Intrumed, Inc. include INSTRUTAINER.