Pascall Medical Corp.
Country not established
- Devices
- 1
What Pascall Medical Corp. makes
Pascall Medical Corp. manufactures the SPIVE Needle System Modification, a device designed for spinal interventions, including procedures such as spinal injections or biopsies.
The company’s portfolio is regulated under FDA Class II devices, with the SPIVE Needle System Modification authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Spive Needle System, Modification Ref K904013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pascall Medical Corp. have in the registry?
The registry currently lists 1 device for Pascall Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pascall Medical Corp.'s devices?
Among its 1 most recently registered device, Pascall Medical Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Pascall Medical Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pascall Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pascall Medical Corp. in the registry?
The most recently registered devices listed for Pascall Medical Corp. include SPIVE NEEDLE SYSTEM, MODIFICATION.