Bentley Laboratories, Inc. - FDA 510(k) Cleared Devices

Bentley Laboratories, Inc. is located in McHenry, US. The company has a historical record of FDA 510(k) device clearances spanning from 1976 to 1993.

Bentley Laboratories received 55 FDA 510(k) clearances from 55 total submissions. The company specialized primarily in Cardiovascular devices, which represented approximately 80% of its regulatory submissions. Notable cleared devices included blood cardioplegia heat exchangers, venous reservoir bags, membrane oxygenators, and central venous catheters used in cardiac surgery and perfusion applications.

The company is inactive and should be treated as a historical regulatory record. No clearances have been granted since 1993. For detailed information on specific device names, product codes, and individual clearance dates, please review the complete 510(k) submission history.