OXYGUARD
Jan 1992
65d
Stantex Pty , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Sydney, New South Wales, AU.
Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Stantex Pty , Ltd. Filter by specialty or product code using the sidebar.