Cruzar Medsystems, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 9
What Cruzar Medsystems, Inc. makes
Cruzar Medsystems, Inc. manufactures the Houdini Catheter and the Houdini Cross Support Catheter, both of which are catheter‑type medical devices used in interventional procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
Houdini Catheter Ref K151896
510(k) 510(k)Houdini Cross Support Catheter Ref K213466
510(k) 510(k)
Company details
- DUNS number
- 080338871
Frequently asked questions
How many devices does Cruzar Medsystems, Inc. have in the registry?
The registry currently lists 9 devices for Cruzar Medsystems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cruzar Medsystems, Inc.'s devices?
Among its 9 most recently registered devices, Cruzar Medsystems, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cruzar Medsystems, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Cruzar Medsystems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cruzar Medsystems, Inc. in the registry?
The most recently registered devices listed for Cruzar Medsystems, Inc. include Cruzar Medsystems Inc. CM-3500, Cruzar Medsystems Inc. CM-3602, Cruzar Medsystems Inc. CM-3800 and Cruzar Medsystems Inc. CM-3400.