Armstrong Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Impulse Hvg Ref K970847
Regimes: 510(k) Registry: 510(k)Sterling Tens Ref K891118
Regimes: 510(k) Registry: 510(k)Simplex Tens Ref K953982
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Armstrong Industries, Inc. have in the registry?
The registry currently lists 3 devices for Armstrong Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Armstrong Industries, Inc.'s devices?
Among its 3 most recently registered devices, Armstrong Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Armstrong Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Armstrong Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Armstrong Industries, Inc. in the registry?
The most recently registered devices listed for Armstrong Industries, Inc. include IMPULSE HVG, STERLING TENS and SIMPLEX TENS.