
Ge Medical Systems Information Technologies
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FETAL MONITOR MODEL 112 is an FDA 510(k)-cleared medical device (K780177) manufactured by Ge Medical Systems Information Technologies. 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 March 1, 1978. Regulation: 8.

Ansell
SKU MSC846624

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SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031