Nordson Efd is one of 21643 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nordson Efd - FDA 510(k) Cleared Devices
Recent clearances: XPRESSE INJECTION SYSTEM
1
Total
1
Cleared
0
Denied
Nordson Efd has 1 FDA 510(k) cleared medical devices. Based in East Providence, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nordson Efd 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 - Nordson Efd
1 devices