Magnatek C-300

K981310 is the FDA 510(k) clearance record for MAGNATEK C-300, a class II device, cleared for Magna Advanced Technologies, Inc. on 1998-07-09 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 7 510(k) clearances for Magna Advanced Technologies, Inc., from 1998-06-24 to 1999-08-19. As of 2026-09-10, FDA records show no recalls naming K981310.