Rtec
Country not established
- Devices
- 2
What Rtec makes
Rtec manufactures disposable plastic oxygen supply tubes and inhalation therapy assemblies, including intermittent positive pressure breathing (IPPB) devices paired with nebulizers for respiratory care applications.
The company’s products are regulated under FDA’s Class I and Class II categories, with relevant devices listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Oxygen Supply Tube, Disp., Plastic Ref K781231
Regimes: 510(k) Registry: 510(k)Ippb Assembly W/Nebulizer Ref K781232
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rtec have in the registry?
The registry currently lists 2 devices for Rtec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rtec's devices?
Among its 2 most recently registered devices, Rtec has devices listed in FDA 510(k) (2 devices).
What risk classes do Rtec's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rtec's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rtec in the registry?
The most recently registered devices listed for Rtec include OXYGEN SUPPLY TUBE, DISP., PLASTIC and IPPB ASSEMBLY W/NEBULIZER.