Alizor, Inc. Dba Global Tech is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alizor, Inc. Dba Global Tech - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Alizor, Inc. Dba Global Tech has 1 FDA 510(k) cleared medical devices. Based in Santa Rosa, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Alizor, Inc. Dba Global Tech Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alizor, Inc. Dba Global Tech
1 devices