Acrew Imaging, Inc.
Country not established
- Devices
- 1
What Acrew Imaging, Inc. makes
Acrew Imaging, Inc. manufactures the F3, a medical imaging device designed for specific diagnostic applications, including high-resolution imaging capabilities for internal structures.
The F3 is classified as a Class II device under FDA regulations and is authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
F3 Ref K222998
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acrew Imaging, Inc. have in the registry?
The registry currently lists 1 device for Acrew Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acrew Imaging, Inc.'s devices?
Among its 1 most recently registered device, Acrew Imaging, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Acrew Imaging, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Acrew Imaging, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acrew Imaging, Inc. in the registry?
The most recently registered devices listed for Acrew Imaging, Inc. include F3.