STRYKER SYSTEM 4000 HEAVY DUTY BATTERY POWERED EQUIPMENT

STRYKER SYSTEM 4000 HEAVY DUTY BATTERY POWERED EQUIPMENT is an FDA 510(k)-cleared medical device (K972367) manufactured by Stryker Instruments. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 3, 1997. Regulation: 8.