Medi-Swiss Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Medi-Swiss Corp. makes
Medi-Swiss Corp. manufactures blood pressure measurement devices, including manual sphygmomanometers like the PRESS-O-TEST and digital monitors such as the EURO-DIAGNOSTIC BLOOD PRESSURE MONITOR, designed for clinical and home use.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Press-O-Test Ref K822102
Regimes: 510(k) Registry: 510(k)Euro-Diagnostic Blood Pressure Monitor Ref K904298
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi-Swiss Corp. have in the registry?
The registry currently lists 2 devices for Medi-Swiss Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Swiss Corp.'s devices?
Among its 2 most recently registered devices, Medi-Swiss Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medi-Swiss Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medi-Swiss Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Swiss Corp. in the registry?
The most recently registered devices listed for Medi-Swiss Corp. include PRESS-O-TEST and EURO-DIAGNOSTIC BLOOD PRESSURE MONITOR.