Madaus Medtec, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Madaus Medtec, Inc. makes
Madaus Medtec, Inc. manufactures MESAM and MESAMIV recorders, which are medical devices designed for monitoring and recording specific physiological data, likely related to cardiac or neurological diagnostics.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Mesam Recorder Ref K894641
Regimes: 510(k) Registry: 510(k)Mesamiv Recorder Ref K901466
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Madaus Medtec, Inc. have in the registry?
The registry currently lists 2 devices for Madaus Medtec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Madaus Medtec, Inc.'s devices?
Among its 2 most recently registered devices, Madaus Medtec, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Madaus Medtec, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Madaus Medtec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Madaus Medtec, Inc. in the registry?
The most recently registered devices listed for Madaus Medtec, Inc. include MESAM RECORDER and MESAMIV RECORDER.