Crs Medical Diagnostics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Crs Medical Diagnostics, Inc. makes
Crs Medical Diagnostics, Inc. manufactures diagnostic devices for assessing fibrin properties within blood vessels, including an endoluminal brush system and a catheter-based testing system designed for intravascular analysis.
These devices are classified as Class II under US regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Fibrin Analysis System Endoluminal Brush Ref K050889
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Crs Medical Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Crs Medical Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crs Medical Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Crs Medical Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Crs Medical Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Crs Medical Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Crs Medical Diagnostics, Inc. in the registry?
The most recently registered devices listed for Crs Medical Diagnostics, Inc. include FIBRIN ANALYSIS SYSTEM ENDOLUMINAL BRUSH and CRS FIBRIN ANALYSIS CATHETER TESTING SYSTEM (FACTS).