Vortex Medical, Inc. is one of 18972 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vortex Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANGIOVAC CANNULA, VORTEX MEDICAL ANGIOVAC CARDIOPULMONARY BYPASS CIRCUIT, VORTEX CANNULA
3
Total
3
Cleared
0
Denied
Vortex Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Norwell, US.
Historical record: 3 cleared submissions from 2009 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vortex Medical, Inc. 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 - Vortex Medical, Inc.
3 devices