Kma, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Kma, Inc. makes
Kma, Inc. manufactures medical devices including a digital thermometer for fever measurement, a heparin-coated thermodilution catheter for cardiac monitoring, and a flow-directed thermodilution catheter for hemodynamic assessments.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
The Fever-Therm A Therm. Measuring Device Ref K850395
Regimes: 510(k) Registry: 510(k)Heparin Coated Thermodilution Catheter Ref K821099
Regimes: 510(k) Registry: 510(k)Kma Flow Directed Thermodilution Cathete Ref K800836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kma, Inc. have in the registry?
The registry currently lists 3 devices for Kma, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kma, Inc.'s devices?
Among its 3 most recently registered devices, Kma, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Kma, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Kma, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kma, Inc. in the registry?
The most recently registered devices listed for Kma, Inc. include THE FEVER-THERM A THERM. MEASURING DEVICE, HEPARIN COATED THERMODILUTION CATHETER and KMA FLOW DIRECTED THERMODILUTION CATHETE.