
Strenumed, Inc.
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SYSTEM 2000 REPLACEMENT BATTERY, SYSTEM 2000-EXTENDED RUN REPLACEMENT BATTERY is an FDA 510(k)-cleared medical device (K951450) manufactured by Strenumed, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 16, 1995. Regulation: 8.