Emergency Medicine
Country not established
- Devices
- 1
What Emergency Medicine makes
The company manufactures automated gastric lavage devices, designed for emergency decontamination of the stomach in acute poisoning cases.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Automated Gastric Lavage Ref K811061
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emergency Medicine have in the registry?
The registry currently lists 1 device for Emergency Medicine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emergency Medicine's devices?
Among its 1 most recently registered device, Emergency Medicine has devices listed in FDA 510(k) (1 device).
What risk classes do Emergency Medicine's devices fall under?
Among its 1 most recently registered device, the classes recorded for Emergency Medicine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emergency Medicine in the registry?
The most recently registered devices listed for Emergency Medicine include AUTOMATED GASTRIC LAVAGE.