Curative Medical Technology, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Curative Medical Technology, Inc. makes
Curative Medical Technology, Inc. makes the URSA Angiographic Catheter, a device used for angiographic procedures.
The URSA Angiographic Catheter is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Ursa Angiographic Catheter Ref K090427
510(k) 510(k)Ursa Angiographic Catheter Ref K123818
510(k) 510(k)
Frequently asked questions
How many devices does Curative Medical Technology, Inc. have in the registry?
The registry currently lists 2 devices for Curative Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curative Medical Technology, Inc.'s devices?
Among its 2 most recently registered devices, Curative Medical Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Curative Medical Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Curative Medical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curative Medical Technology, Inc. in the registry?
The most recently registered devices listed for Curative Medical Technology, Inc. include URSA ANGIOGRAPHIC CATHETER.