Accuro Technologies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Accuro Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARTHROTAP
1
Total
1
Cleared
0
Denied
Accuro Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Victoria, CA.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Accuro Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accuro Technologies, Inc.
1 devices