Hydromer, Inc.
Country not established
- Devices
- 1
What Hydromer, Inc. makes
Hydromer, Inc. manufactures tracheobronchial suction catheters, designed for airway clearance and respiratory care in clinical settings.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Tracheobronchial Suction Catheter Ref K813209
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hydromer, Inc. have in the registry?
The registry currently lists 1 device for Hydromer, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hydromer, Inc.'s devices?
Among its 1 most recently registered device, Hydromer, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hydromer, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hydromer, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hydromer, Inc. in the registry?
The most recently registered devices listed for Hydromer, Inc. include TRACHEOBRONCHIAL SUCTION CATHETER.