
Research Instruments , Ltd.
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SATURN 3 LASER SYSTEM is an FDA 510(k)-cleared medical device (K060764) manufactured by Research Instruments , 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 March 11, 2007. Regulation: 8.

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