Escalon Medical Corp. is one of 24536 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Escalon Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: VASCUVIEW TAP ULTRASOUND SYSTEM, VASCUVIEW ULTRASOUND SYSTEM, MEGAVISION CPX, MEGAVISION FA, MODEL I AND II
3
Total
3
Cleared
0
Denied
Escalon Medical Corp. has 3 FDA 510(k) cleared medical devices. Based in New Berlin, US.
Historical record: 3 cleared submissions from 2000 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Escalon Medical Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Escalon Medical Corp.
3 devices