Horiba, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Horiba, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Yumizen C1200, Yumizen C1200 Glucose HK, Sodium Electrode, Potassium Electrode, Chloride Electrode
2
Total
2
Cleared
0
Denied
Horiba, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 2002 to 2019. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Horiba, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Horiba, Ltd.
2 devices