Tecno Reusable Bipolar Cables, Model 190-100 and 190-110

K042608 is the FDA 510(k) clearance record for TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110, a class II device, cleared for Tecno Instruments (Pvt.) , Ltd. on 2004-10-18 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 2 510(k) clearances for Tecno Instruments (Pvt.) , Ltd., from 2000-10-19 to 2004-10-18. As of 2026-09-10, FDA records show no recalls naming K042608.