Ep Dynamics, Inc. is one of 19642 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ep Dynamics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LINEBACKER(TM) TRANSSEPTAL INTRODUCER, 53CM / 62CM / 72CM, AIRBLOC TRANSSEPTAL INTRODUCER, 53 CM, MODEL FA001, AIRBLOCK TRANSSEPTAL INTRODUCER, 72 CM ,MODEL FA002
2
Total
2
Cleared
0
Denied
Ep Dynamics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mission Viejo, US.
Historical record: 2 cleared submissions from 2009 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ep Dynamics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ep Dynamics, Inc.
2 devices