
Propper Mfg. Co., Inc.
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ONCE-A-DAY VERTOS TEST PACK is an FDA 510(k)-cleared medical device (K082620) manufactured by Propper Mfg. Co., Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 7, 2009. Regulation: 8.

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