Fogg System Company, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fogg System Company, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Fogg System Patient Monitoring Cables
1
Total
1
Cleared
0
Denied
Fogg System Company, Inc. has 1 FDA 510(k) cleared medical devices. Based in Aurora, US.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Fogg System Company, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Novare Medical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Fogg System Company, Inc.
1 devices