Medical Device Manufacturer · US , Irvine , CA

Toxi-Lab, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Toxi-Lab, Inc. has 5 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 5 cleared submissions from 1990 to 1993. Primary specialty: Toxicology.

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

Toxi-Lab, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Toxi-Lab, Inc.

5 devices

1-5 of 5