Norwich Pharmacal Co.
Country not established
- Devices
- 1
What Norwich Pharmacal Co. makes
Norwich Pharmacal Co. manufactures the VIVONEX Delivery System, a device designed for the topical administration of medications in wound care or dermatological applications.
The VIVONEX Delivery System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Vivonex Delivery System Ref K780415
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Norwich Pharmacal Co. have in the registry?
The registry currently lists 1 device for Norwich Pharmacal Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Norwich Pharmacal Co.'s devices?
Among its 1 most recently registered device, Norwich Pharmacal Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Norwich Pharmacal Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Norwich Pharmacal Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Norwich Pharmacal Co. in the registry?
The most recently registered devices listed for Norwich Pharmacal Co. include VIVONEX DELIVERY SYSTEM.