Cygnet Co., Inc.
Country not established
- Devices
- 1
What Cygnet Co., Inc. makes
Cygnet Co., Inc. manufactures the CYGNET CENTRAL, a medical device designed for central venous catheter management and monitoring.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cygnet Central Ref K903992
510(k) 510(k)
Frequently asked questions
How many devices does Cygnet Co., Inc. have in the registry?
The registry currently lists 1 device for Cygnet Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cygnet Co., Inc.'s devices?
Among its 1 most recently registered device, Cygnet Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cygnet Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cygnet Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cygnet Co., Inc. in the registry?
The most recently registered devices listed for Cygnet Co., Inc. include CYGNET CENTRAL.