Snowden Pencer Laparoscopic Ergonomic Reposable Scissors

K113407 is the FDA 510(k) clearance record for SNOWDEN PENCER LAPAROSCOPIC ERGONOMIC REPOSABLE SCISSORS, a class II device, cleared for Carefusion 2200, Inc. on 2012-09-07 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 1,525 510(k) clearances for Medtronic, Inc., from 1976-08-23 to 2026-08-13. As of 2026-09-10, FDA records show no recalls naming K113407.