Pioneer Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pioneer Pro-Pump Ref K914220
Regimes: 510(k) Registry: 510(k)Pioneer Pro-Pump Dual Control Ref K914241
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pioneer Medical, Inc. have in the registry?
The registry currently lists 2 devices for Pioneer Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pioneer Medical, Inc.'s devices?
Among its 2 most recently registered devices, Pioneer Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pioneer Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pioneer Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pioneer Medical, Inc. in the registry?
The most recently registered devices listed for Pioneer Medical, Inc. include PIONEER PRO-PUMP and PIONEER PRO-PUMP DUAL CONTROL.