Entracon Corp. is one of 25969 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Entracon Corp. - FDA 510(k) Cleared Devices
Recent clearances: SENTINEL ENTERAL FEEDING PUMP, LH2001 ENTERAL FEEDING PUMP
1
Total
1
Cleared
0
Denied
Entracon Corp. has 1 FDA 510(k) cleared medical devices. Based in Foxborough, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Entracon Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Entracon Corp.
1 devices