Mti Corp./ Electrostar S.A.-Haiti
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- Devices
- 1
What Mti Corp./ Electrostar S.A.-Haiti makes
Mti Corp./Electrostar S.A.-Haiti manufactures the DUOSTAR, a Class II medical device designed for electrophysiological applications, likely used in cardiac procedures to map or ablate heart tissue.
The DUOSTAR is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Duostar Ref K974170
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mti Corp./ Electrostar S.A.-Haiti have in the registry?
The registry currently lists 1 device for Mti Corp./ Electrostar S.A.-Haiti. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mti Corp./ Electrostar S.A.-Haiti's devices?
Among its 1 most recently registered device, Mti Corp./ Electrostar S.A.-Haiti has devices listed in FDA 510(k) (1 device).
What risk classes do Mti Corp./ Electrostar S.A.-Haiti's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mti Corp./ Electrostar S.A.-Haiti's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mti Corp./ Electrostar S.A.-Haiti in the registry?
The most recently registered devices listed for Mti Corp./ Electrostar S.A.-Haiti include DUOSTAR.