Medical Device Manufacturer · US , Baton Rouge , LA

Geno Laboratories - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1991

Total

Cleared

Denied

Geno Laboratories has 1 FDA 510(k) cleared medical devices. Based in Baton Rouge, US.

Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: General & Plastic Surgery.

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

Geno Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Geno Laboratories

1 devices

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