
General Electric Co.
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5 MHZ INTRACAVITARY PROBE, MODEL H4222V is an FDA 510(k)-cleared medical device (K860233) manufactured by General Electric 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 June 1, 1986. Regulation: 8.

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