Steri-Aid, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Steri-Aid, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Steri-Aid, Inc. has 1 FDA 510(k) cleared medical devices. Based in North York,Ontario, CA.
Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Steri-Aid, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Steri-Aid, Inc.
1 devices