Chiron Corp. is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chiron Corp. - FDA 510(k) Cleared Devices
Recent clearances: ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER ANTIGEN 27.29), ACS 180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM)
2
Total
2
Cleared
0
Denied
Chiron Corp. has 2 FDA 510(k) cleared medical devices. Based in Emeryville, US.
Historical record: 2 cleared submissions from 1998 to 1998. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Chiron Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chiron Corp.
2 devices