
Church & Dwight Co., Inc.
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NIRVANA D PERSONAL LUBRICANT (TBD) is an FDA 510(k)-cleared medical device (K123427) manufactured by Church & Dwight Co., 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 27, 2013. Regulation: 8.

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