Akonni Biosystems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akonni Biosystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TruDiagnosis System
1
Total
1
Cleared
0
Denied
Akonni Biosystems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Frederick, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Akonni Biosystems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MethodSense, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Akonni Biosystems, Inc.
1 devices