Celera Diagnostics is one of 16336 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Celera Diagnostics - FDA 510(k) Cleared Devices
Recent clearances: CYSTIC FIBROSIS GENOTYPING ASSAY, MODEL 6L20-01
1
Total
1
Cleared
0
Denied
Celera Diagnostics has 1 FDA 510(k) cleared medical devices. Based in Alameda, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Celera Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Celera Diagnostics
1 devices