Medical Device Manufacturer · US , Irvine , CA

Horiba, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002
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: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Horiba, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Horiba, Ltd.

2 devices
1-2 of 2
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