Nasorcap Ent., Inc.
Country not established
- Devices
- 1
What Nasorcap Ent., Inc. makes
Nasorcap Ent., Inc. manufactures a nasal/oral oxygen delivery and gas sampling device designed for precise administration and monitoring of respiratory gases in clinical settings.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Nasal/Oral 02 Delivery And Gas Sampling Device Ref K911970
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nasorcap Ent., Inc. have in the registry?
The registry currently lists 1 device for Nasorcap Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nasorcap Ent., Inc.'s devices?
Among its 1 most recently registered device, Nasorcap Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nasorcap Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nasorcap Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nasorcap Ent., Inc. in the registry?
The most recently registered devices listed for Nasorcap Ent., Inc. include NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE.