K.Bowmed, Inc.
Country not established
- Devices
- 1
What K.Bowmed, Inc. makes
K.Bowmed, Inc. makes medical devices such as neonatal restraint and comfort systems.
The company's portfolio is regulated as Class I devices and is listed in the FDA 510k registry, with the company based in the US.
Catalogue
Neonatal Restraint And Comfort Systems Ref K943017
510(k) 510(k)
Frequently asked questions
How many devices does K.Bowmed, Inc. have in the registry?
The registry currently lists 1 device for K.Bowmed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K.Bowmed, Inc.'s devices?
Among its 1 most recently registered device, K.Bowmed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do K.Bowmed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for K.Bowmed, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from K.Bowmed, Inc. in the registry?
The most recently registered devices listed for K.Bowmed, Inc. include NEONATAL RESTRAINT AND COMFORT SYSTEMS.