ARM AUTOMATIC REPROCESSING MACHINE
Jul 2002
249d
Alcavis International Incorporated has 1 FDA 510(k) cleared medical devices. Based in Gaithersburg, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Alcavis International Incorporated Filter by specialty or product code using the sidebar.