Electrophoresis Corp. of America - FDA 510(k) Cleared Devices
Recent clearances: GENERAL PROCEDURE AGAROSE FILM, AGAROSE BARBITAL BUFFER, ALKALINE PHOSPHATASE MARKER
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Electrophoresis Corp. of America Hematology ✕
3 devices