
Telectronics Pacing Systems, Inc.
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MODIFIED J-STIFFENER WIRE MATERIAL IN LEAD LINES is an FDA 510(k)-cleared medical device (K897067) manufactured by Telectronics Pacing Systems, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on February 4, 1990. Regulation: 8.

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