Pst, Inc.
Country not established
- Devices
- 1
What Pst, Inc. makes
Pst, Inc. manufactures electrosurgical generators and bipolar forceps, including the Model 2150 electrosurgical generator and the Model EBF 1228 bipolar forceps, designed for surgical procedures requiring precise tissue cutting and coagulation.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pst, Inc. have in the registry?
The registry currently lists 1 device for Pst, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pst, Inc.'s devices?
Among its 1 most recently registered device, Pst, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pst, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pst, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pst, Inc. in the registry?
The most recently registered devices listed for Pst, Inc. include PST ELECTROSURGICAL GENERATOR, MODEL 2150, PST BIPOLAR FORCEPS, MODEL EBF 1228.