
Panatrex, Inc.
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VAG O SPECULUM, MODELS VS1, VM1, VL1 is an FDA 510(k)-cleared medical device (K042950) manufactured by Panatrex, 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 November 29, 2004. Regulation: 8.

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