Dr. Oliver Wenker, M.D., M.B.A.
Country not established
- Devices
- 1
What Dr. Oliver Wenker, M.D., M.B.A. makes
Dr. Oliver Wenker, M.D., M.B.A. manufactures the FUTURA, a medical device designed for [specific clinical application or purpose not provided in the data]. The product is intended for [brief, implied use, e.g., surgical, diagnostic, or therapeutic procedures] within its designated category.
The FUTURA is classified as a Class II device under FDA regulations and has been submitted for 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Futura Ref K102524
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dr. Oliver Wenker, M.D., M.B.A. have in the registry?
The registry currently lists 1 device for Dr. Oliver Wenker, M.D., M.B.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Oliver Wenker, M.D., M.B.A.'s devices?
Among its 1 most recently registered device, Dr. Oliver Wenker, M.D., M.B.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. Oliver Wenker, M.D., M.B.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. Oliver Wenker, M.D., M.B.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Oliver Wenker, M.D., M.B.A. in the registry?
The most recently registered devices listed for Dr. Oliver Wenker, M.D., M.B.A. include FUTURA.