Valley West, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
1000 Pressure Infusion Sigmacon 1000 Ref K990447
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Trump-It Ii And Magnum 250 Ref K973814
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Valley West, Inc. have in the registry?
The registry currently lists 3 devices for Valley West, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Valley West, Inc.'s devices?
Among its 3 most recently registered devices, Valley West, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Valley West, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Valley West, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Valley West, Inc. in the registry?
The most recently registered devices listed for Valley West, Inc. include 1000 PRESSURE INFUSION SIGMACON 1000, 3600 PRESURE INFUSOR, SIGMACON 3600, LAPRO FLOW 3000 and TRUMP-IT II AND MAGNUM 250.