Pressure-Tech, Inc.
Country not established
- Devices
- 1
What Pressure-Tech, Inc. makes
Pressure-Tech, Inc. manufactures the FLEXI-LITE, which is a medical device.
The company is based in the United States, and its portfolio includes Class II devices that are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Flexi-Lite Ref K101262
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pressure-Tech, Inc. have in the registry?
The registry currently lists 1 device for Pressure-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pressure-Tech, Inc.'s devices?
Among its 1 most recently registered device, Pressure-Tech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pressure-Tech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pressure-Tech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pressure-Tech, Inc. in the registry?
The most recently registered devices listed for Pressure-Tech, Inc. include FLEXI-LITE.