
Katecho, Inc.
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K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60 is an FDA 510(k)-cleared medical device (K991007) manufactured by Katecho, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on August 22, 1999. Regulation: 8.

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