Annidis Health Systems Corp. is one of 511 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Annidis Health Systems Corp. - FDA 510(k) Cleared Devices
Recent clearances: RHA2020
1
Total
1
Cleared
0
Denied
Annidis Health Systems Corp. has 1 FDA 510(k) cleared medical devices. Based in Ottawa, Ontario, CA.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Annidis Health Systems 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 - Annidis Health Systems Corp.
1 devices