Novaste Corp.
Country not established
- Devices
- 1
What Novaste Corp. makes
Novaste Corp. manufactures the Novoste Vessel Dilater, a device designed for vascular dilation procedures to facilitate blood flow in specific medical applications.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Novoste Vessel Dilater Ref K912050
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Novaste Corp. have in the registry?
The registry currently lists 1 device for Novaste Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novaste Corp.'s devices?
Among its 1 most recently registered device, Novaste Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Novaste Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Novaste Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novaste Corp. in the registry?
The most recently registered devices listed for Novaste Corp. include NOVOSTE VESSEL DILATER.