Panion & BF Biotech, Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Panion & BF Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vstrip H. pylori Antigen Rapid Test
1
Total
1
Cleared
0
Denied
Panion & BF Biotech, Inc. has 1 FDA 510(k) cleared medical devices. Based in New Taipei City, TW.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Panion & BF Biotech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Amarex Clinical Research, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Panion & BF Biotech, Inc.
1 devices