Beckman is one of 13022 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beckman - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206, SYNCHRON SYUSTEMS DAT DRUG FREE URINE CONTROL
Beckman, is a diagnostic device manufacturer with a manufacturing facility in Brea, US. The company specializes in chemistry devices, immunoassay systems, and clinical laboratory analyzers.
Beckman received 6 FDA 510(k) clearances from 6 total submissions between 1989 and 1999. The company's cleared devices span chemistry, immunology, and toxicology disciplines. This regulatory record reflects the company's historical focus on clinical laboratory diagnostics.
The company is inactive and maintains a historical record only. No FDA 510(k) clearances have been submitted since 1999. Explore the device names, product codes, and clearance dates in the full 510(k) database.