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Summit Doppler Systems, Inc.
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ECHOHEART TRANSVAGINAL DOPPLER PROBE is an FDA 510(k)-cleared medical device (K060410) manufactured by Summit Doppler Systems, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 2006. Regulation: 8.

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