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

Erika, Inc. is a medical device company based in McHenry, US. The company specialized in Gastroenterology & Urology devices.

Erika, Inc. received 43 FDA 510(k) clearances from 43 total submissions between 1976 and 1985. The company's regulatory focus centered on Gastroenterology & Urology devices, which represented 86% of its submission portfolio. Notable cleared products included infusion pump administration sets, artificial kidney filtration systems, and bicarbonate concentrate formulations.

This company is inactive and represents a historical regulatory record. No FDA 510(k) clearances have been issued since 1985. Explore the complete device names, product codes, and clearance dates in the database.