
Midmark Corp.
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MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR is an FDA 510(k)-cleared medical device (K894335) manufactured by Midmark Corp.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 11, 1989. Regulation: 8.

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