MARINA MEDICAL SILICONE PESSARY

MARINA MEDICAL SILICONE PESSARY is an FDA 510(k)-cleared medical device (K031463) manufactured by Marina Medical Instruments, 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 17, 2003. Regulation: 8.