Diagnostic Data, Inc.
Country not established
- Devices
- 1
What Diagnostic Data, Inc. makes
Diagnostic Data, Inc. manufactures the BONART ART-E1 Electrosurgery Unit, a device designed for controlled tissue cutting and coagulation in surgical procedures.
The BONART ART-E1 Electrosurgery Unit is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Bonart Art-E1 Electrosurgery Unit Ref K020080
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Data, Inc. have in the registry?
The registry currently lists 1 device for Diagnostic Data, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Data, Inc.'s devices?
Among its 1 most recently registered device, Diagnostic Data, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Diagnostic Data, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Diagnostic Data, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Data, Inc. in the registry?
The most recently registered devices listed for Diagnostic Data, Inc. include BONART ART-E1 ELECTROSURGERY UNIT.