Oncopatch, Inc.
Country not established
- Devices
- 1
What Oncopatch, Inc. makes
Oncopatch, Inc. manufactures the OncoPatch, a medical device designed for localized tumor treatment, likely involving targeted drug delivery or radiation therapy enhancement.
The OncoPatch is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
OncoPatch Ref K252296
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oncopatch, Inc. have in the registry?
The registry currently lists 1 device for Oncopatch, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oncopatch, Inc.'s devices?
Among its 1 most recently registered device, Oncopatch, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Oncopatch, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oncopatch, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oncopatch, Inc. in the registry?
The most recently registered devices listed for Oncopatch, Inc. include OncoPatch.