Oxypulse
Country not established
- Devices
- 1
What Oxypulse makes
Oxypulse manufactures fingertip pulse oximeters, including the OXIBLUE and OXIPRO models, designed for non-invasive monitoring of blood oxygen saturation and pulse rate.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Oxiblue Fingertip Pulse Oximeter Model MD300C318, Oxipro Fingertip Pulse Oximeter Model MD300C316 Ref K100815
510(k) 510(k)
Frequently asked questions
How many devices does Oxypulse have in the registry?
The registry currently lists 1 device for Oxypulse. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oxypulse's devices?
Among its 1 most recently registered device, Oxypulse has devices listed in FDA 510(k) (1 device).
What risk classes do Oxypulse's devices fall under?
Among its 1 most recently registered device, the classes recorded for Oxypulse's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oxypulse in the registry?
The most recently registered devices listed for Oxypulse include OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE OXIMETER MODEL MD300C316.