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Fischer Industries, Inc.
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LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D is an FDA 510(k)-cleared medical device (K022154) manufactured by Fischer Industries, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 29, 2002. Regulation: 8.