Pneumocare, Inc.
Country not established
- Devices
- 1
What Pneumocare, Inc. makes
Pneumocare, Inc. manufactures disposable tracheostomy tubes, including standard and fenestrated designs with inner cannulas. These devices are intended for long-term airway management in patients requiring tracheostomy care.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements. These devices are listed in the FDA’s 510(k) database and are manufactured in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pneumocare, Inc. have in the registry?
The registry currently lists 1 device for Pneumocare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneumocare, Inc.'s devices?
Among its 1 most recently registered device, Pneumocare, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pneumocare, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pneumocare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneumocare, Inc. in the registry?
The most recently registered devices listed for Pneumocare, Inc. include DISPOSABLE CANNULA TRACHEOSTOMY TUBE, WITH INNER CANNULA;DISPOSABLE CANNULA FENESTRATED TRACHEOSTOMY TUBE, WITH INNER CN.