Agfa Corporation is one of 25255 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Agfa Corporation - FDA 510(k) Cleared Devices
Recent clearances: CR 85-X, AGFA MODEL CR30-X, COMPUTED RADIOGRAPHY SYSTEM WITH NX 1.0 WORKSTATION
4
Total
4
Cleared
0
Denied
Agfa Corporation has 4 FDA 510(k) cleared medical devices. Based in Greenville, US.
Historical record: 4 cleared submissions from 2005 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Agfa Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Agfa Corporation
4 devices