Pci Medical, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
GUS ASTRA TEE Transesophageal Probe Reprocessor, GUS ASTRA VR Endovaginal/Endorectal Probe Reprocessor Ref K150504
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pci Medical, Inc. have in the registry?
The registry currently lists 1 device for Pci Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pci Medical, Inc.'s devices?
Among its 1 most recently registered device, Pci Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pci Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pci Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pci Medical, Inc. in the registry?
The most recently registered devices listed for Pci Medical, Inc. include GUS ASTRA TEE Transesophageal Probe Reprocessor, GUS ASTRA VR Endovaginal/Endorectal Probe Reprocessor.