Murex Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Murex Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Murex Corp. has 5 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 5 cleared submissions from 1986 to 1986. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Murex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Murex Corp.
5 devices
Cleared
Jun 19, 1986
SUDS(HCG)CONTROL SET (URINE&SERUM) & HCG REF.SERUM
Chemistry
21d
Cleared
Jun 13, 1986
MUREX SUDS RUBELLA
Microbiology
67d
Cleared
Jun 13, 1986
MUREX SUDS TOXO
Microbiology
56d
Cleared
Apr 21, 1986
MUREX (TM), SUDS (TM), HCG ASSAY
Chemistry
75d
Cleared
Apr 04, 1986
MUREX SUDS GROUP A STREP
Microbiology
45d