Bruce J. Sand M.D.
Country not established
- Devices
- 1
What Bruce J. Sand M.D. makes
The manufacturer produces the COOLCUBE COOLPEN, a medical device classified as a Class II product.
These devices are regulated under the FDA 510(k) pathway and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Coolcube Coolpen Ref K041767
510(k) 510(k)
Frequently asked questions
How many devices does Bruce J. Sand M.D. have in the registry?
The registry currently lists 1 device for Bruce J. Sand M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bruce J. Sand M.D.'s devices?
Among its 1 most recently registered device, Bruce J. Sand M.D. has devices listed in FDA 510(k) (1 device).
What risk classes do Bruce J. Sand M.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bruce J. Sand M.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bruce J. Sand M.D. in the registry?
The most recently registered devices listed for Bruce J. Sand M.D. include COOLCUBE COOLPEN.