SYSTEM 2000 REPLACEMENT BATTERY, SYSTEM 2000-EXTENDED RUN REPLACEMENT BATTERY
May 1995
49d
Strenumed, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ventura, US.
Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Strenumed, Inc. Filter by specialty or product code using the sidebar.