
Cutter Laboratories, Inc.
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ELC-THERMO-SYSTEM is an FDA 510(k)-cleared medical device (K770678) manufactured by Cutter Laboratories, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 24, 1977. Regulation: 8.

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