Mitchell V. Kaminski, Jr., M.D.
Country not established
- Devices
- 1
What Mitchell V. Kaminski, Jr., M.D. makes
The company designs and manufactures a modified feeding jejunostomy tube, a specialized medical device used for enteral nutrition delivery directly into the jejunum via a surgically created stoma.
This device is classified as Class II under FDA regulations and is listed via a 510(k) premarket notification process. The manufacturer operates from the United States.
Catalogue
Modified Feeding Jejunostomy Tube Ref K800918
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mitchell V. Kaminski, Jr., M.D. have in the registry?
The registry currently lists 1 device for Mitchell V. Kaminski, Jr., M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mitchell V. Kaminski, Jr., M.D.'s devices?
Among its 1 most recently registered device, Mitchell V. Kaminski, Jr., M.D. has devices listed in FDA 510(k) (1 device).
What risk classes do Mitchell V. Kaminski, Jr., M.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mitchell V. Kaminski, Jr., M.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mitchell V. Kaminski, Jr., M.D. in the registry?
The most recently registered devices listed for Mitchell V. Kaminski, Jr., M.D. include MODIFIED FEEDING JEJUNOSTOMY TUBE.