Burkick Corp.
Country not established
- Devices
- 1
What Burkick Corp. makes
Burkick Corp. manufactures the M305, a medical device designed for [specific application not detailed in provided data].
The M305 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
M305 Ref K833819
510(k) 510(k)
Frequently asked questions
How many devices does Burkick Corp. have in the registry?
The registry currently lists 1 device for Burkick Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Burkick Corp.'s devices?
Among its 1 most recently registered device, Burkick Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Burkick Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Burkick Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Burkick Corp. in the registry?
The most recently registered devices listed for Burkick Corp. include M305.