Medical Device Manufacturer · DE , D-79104 Freiburg

Optomotor Laboratories - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Total

Cleared

Denied

Optomotor Laboratories has 1 FDA 510(k) cleared medical devices. Based in D-79104 Freiburg, DE.

Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Neurology.

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

Optomotor Laboratories 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 - Optomotor Laboratories

1 devices

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