Medical Device Manufacturer · US , Oakfield , NY

Nu-Gyn-Tek, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986

Total

Cleared

Denied

Nu-Gyn-Tek, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oakfield, US.

Historical record: 2 cleared submissions from 1986 to 1990. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Nu-Gyn-Tek, Inc. Filter by specialty or product code using the sidebar.

Nu-Gyn-Tek, Inc. 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 - Nu-Gyn-Tek, Inc.

2 devices

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