
Schlosser Alberti Co.
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SA/7860 FETAL HEART MONITOR (DOPPLER) is an FDA 510(k)-cleared medical device (K790951) manufactured by Schlosser Alberti Co.. 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 August 2, 1979. Regulation: 8.

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