Duke University Medical Center
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- Devices
- 1
What Duke University Medical Center makes
Duke University Medical Center manufactures the WEEKS Applicator, a device used in the delivery of radioactive seeds for brachytherapy in prostate cancer treatment.
The WEEKS Applicator is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The institution is based in the United States.
Catalogue
Weeks Applicator Ref K951052
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Duke University Medical Center have in the registry?
The registry currently lists 1 device for Duke University Medical Center. Devices recorded under merged duplicate company entries are counted once.
Which registries list Duke University Medical Center's devices?
Among its 1 most recently registered device, Duke University Medical Center has devices listed in FDA 510(k) (1 device).
What risk classes do Duke University Medical Center's devices fall under?
Among its 1 most recently registered device, the classes recorded for Duke University Medical Center's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Duke University Medical Center in the registry?
The most recently registered devices listed for Duke University Medical Center include WEEKS APPLICATOR.