Cardiovascular Research, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cardiovascular Research, Inc. makes
Cardiovascular Research, Inc. manufactures vascular access devices, including cannula introducers for percutaneous procedures, and extracorporeal membrane oxygenation systems like the Partner Seven Disposable Bubble Oxygenator, designed for temporary cardiac and respiratory support.
These products are classified as Class II medical devices under US regulations and are listed in the FDA’s 510(k) clearance registry. The company operates within the United States.
Catalogue
Cannula Introducer Ref K843118
Regimes: 510(k) Registry: 510(k)Partner Seven Disp. Bubble Oxygenator Ref K800555
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiovascular Research, Inc. have in the registry?
The registry currently lists 2 devices for Cardiovascular Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiovascular Research, Inc.'s devices?
Among its 2 most recently registered devices, Cardiovascular Research, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cardiovascular Research, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cardiovascular Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiovascular Research, Inc. in the registry?
The most recently registered devices listed for Cardiovascular Research, Inc. include CANNULA INTRODUCER and PARTNER SEVEN DISP. BUBBLE OXYGENATOR.