Deseret Pharmaceutical Co.
Country not established
- Devices
- 1
What Deseret Pharmaceutical Co. makes
Deseret Pharmaceutical Co. manufactures electro-surgical devices designed for controlled tissue cutting and coagulation in medical procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Electro-Surgical Devices Ref K771009
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deseret Pharmaceutical Co. have in the registry?
The registry currently lists 1 device for Deseret Pharmaceutical Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deseret Pharmaceutical Co.'s devices?
Among its 1 most recently registered device, Deseret Pharmaceutical Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Deseret Pharmaceutical Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Deseret Pharmaceutical Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deseret Pharmaceutical Co. in the registry?
The most recently registered devices listed for Deseret Pharmaceutical Co. include ELECTRO-SURGICAL DEVICES.