Deeplook, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deeplook, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DeepLook PRECISE
1
Total
1
Cleared
0
Denied
Deeplook, Inc. has 1 FDA 510(k) cleared medical devices. Based in Silver Spring, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Deeplook, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O Tech, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Deeplook, Inc.
1 devices