
Huntleigh Healthcare, Inc.
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MULTI DOPPLEX II / FETAL DOPPLEX II is an FDA 510(k)-cleared medical device (K930200) manufactured by Huntleigh Healthcare, 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 June 23, 1994. Regulation: 8.

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