Medical Device Manufacturer · IT , Belluno

Visard Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Visard Srl has 2 FDA 510(k) cleared medical devices. Based in Belluno, IT.

Historical record: 2 cleared submissions from 1996 to 1996. Primary specialty: Ophthalmic.

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

Visard Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Visard Srl

2 devices

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