Hi-Temp Looptip Surgical Cautery

K802330 is the FDA 510(k) clearance record for HI-TEMP LOOPTIP SURGICAL CAUTERY, a class II device, cleared for Medical Products Development, Inc. on 1980-11-12 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 13 510(k) clearances for Medical Products Development, Inc., from 1980-06-04 to 1981-04-23. As of 2026-09-10, FDA records show no recalls naming K802330.