Med-Western Electronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
View-Lite, Model-S Ref K802215
Regimes: 510(k) Registry: 510(k)Litronic Stimulator Ref K810225
Regimes: 510(k) Registry: 510(k)View-Lite, Model-Sl Ref K802217
Regimes: 510(k) Registry: 510(k)Bio-Stimulator, Model 400 Ref K813100
Regimes: 510(k) Registry: 510(k)View-Lite, Model-Dl Ref K802216
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med-Western Electronics, Inc. have in the registry?
The registry currently lists 5 devices for Med-Western Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-Western Electronics, Inc.'s devices?
Among its 5 most recently registered devices, Med-Western Electronics, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Med-Western Electronics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Med-Western Electronics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med-Western Electronics, Inc. in the registry?
The most recently registered devices listed for Med-Western Electronics, Inc. include VIEW-LITE, MODEL-S, LITRONIC STIMULATOR, VIEW-LITE, MODEL-SL and BIO-STIMULATOR, MODEL 400.