Medical Device Manufacturer · US , South Plainfield , NJ

G.U.-Tek - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

G.U.-Tek has 1 FDA 510(k) cleared medical devices. Based in South Plainfield, US.

Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by G.U.-Tek Filter by specialty or product code using the sidebar.

G.U.-Tek 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 - G.U.-Tek

1 devices

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