Protologic, Inc.
Country not established
- Devices
- 1
What Protologic, Inc. makes
Protologic, Inc. manufactures the Model SER-1, a surgical electrosurgical device designed for tissue ablation and coagulation procedures.
The Model SER-1 is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Protologic Model Ser-1 Ref K894936
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Protologic, Inc. have in the registry?
The registry currently lists 1 device for Protologic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Protologic, Inc.'s devices?
Among its 1 most recently registered device, Protologic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Protologic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Protologic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Protologic, Inc. in the registry?
The most recently registered devices listed for Protologic, Inc. include PROTOLOGIC MODEL SER-1.