
J.K. Chemicals, Ltd.
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LATEX PROPHYLACTIC RUBBER CONTRACEPTIVE is an FDA 510(k)-cleared medical device (K931077) manufactured by J.K. Chemicals, Ltd.. 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 September 13, 1994. Regulation: 8.

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