Neotronics Medical, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Neotronics Medical, Ltd. makes
Neotronics Medical, Ltd. manufactures the ERA 2000 Emergency Resuscitator, a device designed for manual resuscitation in emergency medical situations, providing controlled ventilation to patients.
The ERA 2000 Emergency Resuscitator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance pathway. The company is based in the United States.
Catalogue
Era 2000 Emergency Resuscitator Ref K884089
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neotronics Medical, Ltd. have in the registry?
The registry currently lists 1 device for Neotronics Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neotronics Medical, Ltd.'s devices?
Among its 1 most recently registered device, Neotronics Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Neotronics Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neotronics Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neotronics Medical, Ltd. in the registry?
The most recently registered devices listed for Neotronics Medical, Ltd. include ERA 2000 EMERGENCY RESUSCITATOR.