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Dolphin Medical, Inc.
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DOLPHIN MEDICAL 2150 HANDHELD PULSE OXIMETER is an FDA 510(k)-cleared medical device (K030629) manufactured by Dolphin Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 3, 2003. Regulation: 8.