Kalera Medical, Inc.
Country not established
- Devices
- 1
What Kalera Medical, Inc. makes
Kalera Medical, Inc. manufactures the Kalera Vacuum Aspiration Catheter (K-VAC), a device designed for surgical aspiration of fluids and debris during minimally invasive procedures.
The K-VAC is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Kalera Vacuum Aspiration Catheter (K-VAC) Ref K200419
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kalera Medical, Inc. have in the registry?
The registry currently lists 1 device for Kalera Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kalera Medical, Inc.'s devices?
Among its 1 most recently registered device, Kalera Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kalera Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kalera Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kalera Medical, Inc. in the registry?
The most recently registered devices listed for Kalera Medical, Inc. include Kalera Vacuum Aspiration Catheter (K-VAC).