Bernsco Electrosurgical Shield

K883823 is the FDA 510(k) clearance record for BERNSCO ELECTROSURGICAL SHIELD, a class II device, cleared for Bernsco Surgical Supply, Inc. on 1988-10-04 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 4 510(k) clearances for Bernsco Surgical Supply, Inc., from 1988-10-04 to 1992-11-27. As of 2026-09-10, FDA records show no recalls naming K883823.