Medical Device Manufacturer · US , Irvine , CA

Visiscan - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986
1
Total
1
Cleared
0
Denied

Visiscan has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Visiscan
1 devices
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