Gen Trak, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gen Trak, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Gen Trak, Inc. has 5 FDA 510(k) cleared medical devices. Based in Plymouth Meeting, US.
Historical record: 5 cleared submissions from 1992 to 1992. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Gen Trak, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gen Trak, Inc.
5 devices
Cleared
Jul 28, 1992
MONOMCLONAL ANTIBODY IGG1 ISOTYPE CONT. FLOW CYTOM
Hematology
85d
Cleared
Jul 28, 1992
MONOCLONAL ANTIBODY IGG2A ISOTYPE CONT. FLOW CYTOM
Hematology
85d
Cleared
Jun 19, 1992
CD2 MONOCLONAL ANTIBODIES
Hematology
235d
Cleared
Jun 19, 1992
CD8 MONOCLONAL ANTIBODIES
Hematology
235d
Cleared
Jun 19, 1992
CD4 MONOCLONAL ANTIBODIES
Hematology
235d