
Carter Products
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TROJAN-ENZ LATEX CONDOMS (MODIFIED LABELING) is an FDA 510(k)-cleared medical device (K901191) manufactured by Carter Products. 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 April 15, 1990. Regulation: 8.

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