Wilson Biomedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Wilson Biomedical, Inc. makes
Wilson Biomedical, Inc. manufactures coronary guiding catheters and angiographic catheters, which are used in cardiac catheterization procedures to visualize blood vessels and guide interventional tools during coronary angiography and percutaneous coronary interventions.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Wilson Biomedical Coronary Guiding Catheter Ref K881793
Regimes: 510(k) Registry: 510(k)Wilson Biomedical Angiographic Catheter Ref K892671
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wilson Biomedical, Inc. have in the registry?
The registry currently lists 2 devices for Wilson Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wilson Biomedical, Inc.'s devices?
Among its 2 most recently registered devices, Wilson Biomedical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Wilson Biomedical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wilson Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wilson Biomedical, Inc. in the registry?
The most recently registered devices listed for Wilson Biomedical, Inc. include WILSON BIOMEDICAL CORONARY GUIDING CATHETER and WILSON BIOMEDICAL ANGIOGRAPHIC CATHETER.