
Microlife Corp.
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MICROLIFE ELECTRONIC PEAK FLOW MONITOR, MODEL PF-100 is an FDA 510(k)-cleared medical device (K031024) manufactured by Microlife Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 13, 2003. Regulation: 8.