Eme (Electro Medical Equipment), Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Eme (Electro Medical Equipment), Ltd. makes
Eme (Electro Medical Equipment), Ltd. manufactures the Infant Flow System, Model M672P, which is a respiratory support device designed for neonatal care.
The Infant Flow System, Model M672P is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Infant Flow System, Model M672P Ref K011516
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eme (Electro Medical Equipment), Ltd. have in the registry?
The registry currently lists 1 device for Eme (Electro Medical Equipment), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eme (Electro Medical Equipment), Ltd.'s devices?
Among its 1 most recently registered device, Eme (Electro Medical Equipment), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Eme (Electro Medical Equipment), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eme (Electro Medical Equipment), Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eme (Electro Medical Equipment), Ltd. in the registry?
The most recently registered devices listed for Eme (Electro Medical Equipment), Ltd. include INFANT FLOW SYSTEM, MODEL M672P.