Bistech, Inc.
Country not established
- Devices
- 1
What Bistech, Inc. makes
Bistech, Inc. manufactures dual-lumen catheters, which are medical devices designed for dual-channel fluid management or monitoring in clinical settings.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Dual-Lumen Catheter Ref K024165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bistech, Inc. have in the registry?
The registry currently lists 1 device for Bistech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bistech, Inc.'s devices?
Among its 1 most recently registered device, Bistech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bistech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bistech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bistech, Inc. in the registry?
The most recently registered devices listed for Bistech, Inc. include DUAL-LUMEN CATHETER.