Meco Industries
Country not established
- Devices
- 2
What Meco Industries makes
Meco Industries manufactures the MECTEST device, a diagnostic tool designed for specific medical evaluations. The product appears to be a reusable or single-use instrument intended for clinical testing in a controlled setting, though exact applications are not specified.
The MECTEST device is classified as a Class II medical device under FDA regulations and requires a 510(k) clearance for market authorisation. The company is based in the United States, and the device is listed in the FDA’s 510(k) registry.
Catalogue
Frequently asked questions
How many devices does Meco Industries have in the registry?
The registry currently lists 2 devices for Meco Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meco Industries's devices?
Among its 2 most recently registered devices, Meco Industries has devices listed in FDA 510(k) (2 devices).
What risk classes do Meco Industries's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Meco Industries's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meco Industries in the registry?
The most recently registered devices listed for Meco Industries include MECTEST.