Medical Device Manufacturer · US , La Vista , NE

Streck, Inc. - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 2020

Total

Cleared

Denied

Streck, Inc. has 2 FDA 510(k) cleared medical devices. Based in La Vista, US.

Latest FDA clearance: Jul 2024. Active since 2020. Primary specialty: Chemistry.

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

Streck, 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 - Streck, Inc.

3 devices

1-3 of 3