Intek Int'L, Inc.
Country not established
- Devices
- 1
What Intek Int'L, Inc. makes
Intek Int'L, Inc. makes an air fluid exchange pump.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Air Fluid Exchange Pump Ref K832761
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intek Int'L, Inc. have in the registry?
The registry currently lists 1 device for Intek Int'L, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intek Int'L, Inc.'s devices?
Among its 1 most recently registered device, Intek Int'L, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intek Int'L, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intek Int'L, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intek Int'L, Inc. in the registry?
The most recently registered devices listed for Intek Int'L, Inc. include AIR FLUID EXCHANGE PUMP.