Rapidex of London
United KingdomFDA applicant, unverified
- Devices
- 1
What Rapidex of London makes
Rapidex of London manufactures the RAPIDEX BIOLOGICAL SURFACTANT, a product designed for use in respiratory support and lung surfactant replacement therapy for neonates and infants.
The RAPIDEX BIOLOGICAL SURFACTANT is classified as a Class I medical device under FDA regulations and is listed via a 510(k) submission. The company is based in the United States.
Catalogue
Rapidex Biological Surfactant Ref K862282
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rapidex of London have in the registry?
The registry currently lists 1 device for Rapidex of London. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rapidex of London's devices?
Among its 1 most recently registered device, Rapidex of London has devices listed in FDA 510(k) (1 device).
What risk classes do Rapidex of London's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rapidex of London's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rapidex of London in the registry?
The most recently registered devices listed for Rapidex of London include RAPIDEX BIOLOGICAL SURFACTANT.