Vasocor, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Vasocor, Inc. makes
Vasocor, Inc. manufactures vascular diagnostic systems, including the VASOCOR Vascular Diagnostic Center (Model 300) and the PVR-100/Vasogram, which are designed for imaging and assessing blood vessels. These devices support intravascular imaging and diagnostic procedures, such as angiography, to evaluate vascular conditions.
The company’s portfolio consists of Class II medical devices, which are regulated under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) database and are intended for use in the United States.
Catalogue
Vasocor Vascular Diagnostic Center (Model 300) Ref K011625
Regimes: 510(k) Registry: 510(k)Pvr-100/Vasogram Ref K990123
Regimes: 510(k) Registry: 510(k)Vasocor Pvr 100 Ref K973659
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vasocor, Inc. have in the registry?
The registry currently lists 3 devices for Vasocor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vasocor, Inc.'s devices?
Among its 3 most recently registered devices, Vasocor, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Vasocor, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vasocor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vasocor, Inc. in the registry?
The most recently registered devices listed for Vasocor, Inc. include VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300), PVR-100/VASOGRAM and VASOCOR PVR 100.