
Davol, Inc.
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AQUASENS FLUID MONITORING SYSTEM is an FDA 510(k)-cleared medical device (K031213) manufactured by Davol, 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 April 29, 2003. Regulation: 8.

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