A.M.I. Corp.
Country not established
- Devices
- 1
What A.M.I. Corp. makes
A.M.I. Corp. manufactures the AMI E-Z-PACE Electrode, a device designed for pacing and monitoring cardiac activity, facilitating temporary cardiac pacing in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with the AMI E-Z-PACE Electrode listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Ami E-Z-Pace Electode Ref K854924
510(k) 510(k)
Frequently asked questions
How many devices does A.M.I. Corp. have in the registry?
The registry currently lists 1 device for A.M.I. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list A.M.I. Corp.'s devices?
Among its 1 most recently registered device, A.M.I. Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do A.M.I. Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for A.M.I. Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A.M.I. Corp. in the registry?
The most recently registered devices listed for A.M.I. Corp. include AMI E-Z-PACE ELECTODE.