Medifield, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Medifield, Ltd. makes
Medifield, Ltd. manufactures the HILT-WAY Resuscitator, a manual resuscitation device designed for emergency use in cardiac arrest or respiratory failure scenarios.
The HILT-WAY Resuscitator is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
'hilt-Way' Resuscitator Ref K880241
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medifield, Ltd. have in the registry?
The registry currently lists 1 device for Medifield, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medifield, Ltd.'s devices?
Among its 1 most recently registered device, Medifield, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medifield, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medifield, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medifield, Ltd. in the registry?
The most recently registered devices listed for Medifield, Ltd. include 'HILT-WAY' RESUSCITATOR.