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Brentwood Medical Technology Corp.
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BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH MOUTHPIECES AND 3-LITER CALIBRATION SYRINGE is an FDA 510(k)-cleared medical device (K002499) manufactured by Brentwood Medical Technology 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 7, 2000. Regulation: 8.
