Acrew Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acrew Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: F3
1
Total
1
Cleared
0
Denied
Acrew Imaging, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ocean View, US.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Acrew Imaging, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Yolanda Smith as regulatory consultant.
FDA 510(k) Regulatory Record - Acrew Imaging, Inc.
1 devices