ADI SYPHILIS RPR LIQUID CONTROLS
Jul 1998
137d
Ampcor Diagnostics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Bridgeport, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Ampcor Diagnostics, Inc.Filter by specialty or product code using the sidebar.