Efilm Medical, Inc. is one of 691 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Efilm Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EFILM WORKSTATION WITH MODULES, EFILM VIDEO, EFILM WORKSTATION
3
Total
3
Cleared
0
Denied
Efilm Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Toronto, Ontario, CA.
Historical record: 3 cleared submissions from 2001 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Efilm Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Efilm Medical, Inc.
3 devices