Ovutime, Inc.
Country not established
- Devices
- 1
What Ovutime, Inc. makes
Ovutime, Inc. manufactures a mucus aspirator, a device designed for the removal of mucus from the respiratory tract, commonly used in neonatal and pediatric care settings.
The company’s mucus aspirator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The device is regulated under US jurisdiction.
Catalogue
Mucus Aspirator Ref K781917
510(k) 510(k)
Frequently asked questions
How many devices does Ovutime, Inc. have in the registry?
The registry currently lists 1 device for Ovutime, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ovutime, Inc.'s devices?
Among its 1 most recently registered device, Ovutime, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ovutime, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ovutime, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ovutime, Inc. in the registry?
The most recently registered devices listed for Ovutime, Inc. include MUCUS ASPIRATOR.