Arteria Medical Science, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Arteria Medical Science, Inc. makes
Arteria Medical Science, Inc. manufactures vascular devices including the Arteria Blood Filter, designed for removing emboli during procedures; the Parodi Catheter for Angiography (PARCA), used in diagnostic coronary angiography; and the Arteria Occlusion Balloon, intended for temporary vessel occlusion during interventional radiology.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is headquartered in the United States.
Catalogue
Arteria Blood Filter Ref K021293
Regimes: 510(k) Registry: 510(k)Parodi Catheter For Angiography (Parca) Ref K001917
Regimes: 510(k) Registry: 510(k)Arteria Occlusion Balloon Ref K021210
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arteria Medical Science, Inc. have in the registry?
The registry currently lists 3 devices for Arteria Medical Science, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arteria Medical Science, Inc.'s devices?
Among its 3 most recently registered devices, Arteria Medical Science, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Arteria Medical Science, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Arteria Medical Science, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arteria Medical Science, Inc. in the registry?
The most recently registered devices listed for Arteria Medical Science, Inc. include ARTERIA BLOOD FILTER, PARODI CATHETER FOR ANGIOGRAPHY (PARCA) and ARTERIA OCCLUSION BALLOON.