Bunkerhill, Inc.
Country not established
- Devices
- 1
What Bunkerhill, Inc. makes
Bunkerhill, Inc. manufactures the iCAC Device, a Class II medical device designed for critical care applications, likely involving cardiac or circulatory support functions.
The iCAC Device is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
iCAC Device Ref K230223
510(k) 510(k)
Frequently asked questions
How many devices does Bunkerhill, Inc. have in the registry?
The registry currently lists 1 device for Bunkerhill, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bunkerhill, Inc.'s devices?
Among its 1 most recently registered device, Bunkerhill, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bunkerhill, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bunkerhill, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bunkerhill, Inc. in the registry?
The most recently registered devices listed for Bunkerhill, Inc. include iCAC Device.