Medical Device Manufacturer · DE , Kelkheim

Siegel Optik - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Siegel Optik has 1 FDA 510(k) cleared medical devices. Based in Kelkheim, DE.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.

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

Siegel Optik is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Siegel Optik

1 devices

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