
Gynecare, Inc.
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GYNECARE VERSAPOINT G-VAP ELECTRODE is an FDA 510(k)-cleared medical device (K992901) manufactured by Gynecare, 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 January 17, 2000. Regulation: 8.

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