E.A. Fischione Instrument Mfg. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
E.A. Fischione Instrument Mfg. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
E.A. Fischione Instrument Mfg. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1984 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by E.A. Fischione Instrument Mfg. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - E.A. Fischione Instrument Mfg.
2 devices