Murex Diagnostics, Inc. is one of 11597 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Murex Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WELLCOLEX E-COLI OI57 ZC60, MUREX RUB-EX
2
Total
2
Cleared
0
Denied
Murex Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 2 cleared submissions from 1996 to 1996. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Murex Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Murex Diagnostics, Inc.
2 devices