Cerasys, Inc.
Country not established
- Devices
- 1
What Cerasys, Inc. makes
Cerasys, Inc. manufactures the CERASYS-ZR, a medical device designed for use in specific surgical or diagnostic procedures, though the exact application is not specified in the provided data.
The CERASYS-ZR is classified as a Class II device under FDA regulations and has been authorised through the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Cerasys - Zr Ref K042548
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cerasys, Inc. have in the registry?
The registry currently lists 1 device for Cerasys, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cerasys, Inc.'s devices?
Among its 1 most recently registered device, Cerasys, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cerasys, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cerasys, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cerasys, Inc. in the registry?
The most recently registered devices listed for Cerasys, Inc. include CERASYS - ZR.