Hemodynamics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Hemodynamics, Inc. makes
Hemodynamics, Inc. manufactures the LEUNOMED RFB 5000, a device for measuring blood flow and vascular resistance, and Light Reflection Rheography, a non-invasive method for assessing peripheral blood circulation and vascular reactivity.
The company’s portfolio consists of Class II medical devices, authorised via FDA 510(k) clearance, and is based in the United States.
Catalogue
Leunomed Rfb 5000 Ref K881164
Regimes: 510(k) Registry: 510(k)Light Reflection Rheography Ref K852378
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemodynamics, Inc. have in the registry?
The registry currently lists 2 devices for Hemodynamics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemodynamics, Inc.'s devices?
Among its 2 most recently registered devices, Hemodynamics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hemodynamics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hemodynamics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemodynamics, Inc. in the registry?
The most recently registered devices listed for Hemodynamics, Inc. include LEUNOMED RFB 5000 and LIGHT REFLECTION RHEOGRAPHY.