Pd International AB
SwedenFDA applicant, unverified
- Devices
- 1
What Pd International AB makes
Pd International AB manufactures peri probe components, including probe tips and peri probe assemblies designed for medical imaging and diagnostic procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Probe Tip/Peri Probe/Peri Probe Comp. Ref K936221
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pd International AB have in the registry?
The registry currently lists 1 device for Pd International AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pd International AB's devices?
Among its 1 most recently registered device, Pd International AB has devices listed in FDA 510(k) (1 device).
What risk classes do Pd International AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pd International AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pd International AB in the registry?
The most recently registered devices listed for Pd International AB include PROBE TIP/PERI PROBE/PERI PROBE COMP..