Vascor, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Vascor, Inc. makes
Vascor, Inc. manufactures disposable holders designed for use with Hancock aortic and mitral heart valves, facilitating surgical handling and positioning during valve replacement procedures.
These products are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Disposable Holder For Hancock Aortic Ref K811236
Regimes: 510(k) Registry: 510(k)Disposable Holder For Hancock Mitral Ref K811235
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascor, Inc. have in the registry?
The registry currently lists 2 devices for Vascor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascor, Inc.'s devices?
Among its 2 most recently registered devices, Vascor, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vascor, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vascor, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vascor, Inc. in the registry?
The most recently registered devices listed for Vascor, Inc. include DISPOSABLE HOLDER FOR HANCOCK AORTIC and DISPOSABLE HOLDER FOR HANCOCK MITRAL.