Mabco, Inc.
AustriaFDA applicant, unverified
- Devices
- 1
What Mabco, Inc. makes
Mabco, Inc. manufactures the DIMERTEST LATEX device.
The DIMERTEST LATEX is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dimertest Latex Ref K842277
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mabco, Inc. have in the registry?
The registry currently lists 1 device for Mabco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mabco, Inc.'s devices?
Among its 1 most recently registered device, Mabco, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mabco, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mabco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mabco, Inc. in the registry?
The most recently registered devices listed for Mabco, Inc. include DIMERTEST LATEX.