Premier Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Premier Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OralTox Oral fluid Drug Test, OralTox Oral Fluid Drug Test
2
Total
2
Cleared
0
Denied
Premier Biotech, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Premier Biotech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Premier Biotech, Inc.
2 devices