454A Electrosurgical Analyzer

K942627 is the FDA 510(k) clearance record for 454A ELECTROSURGICAL ANALYZER, a class II device, cleared for Hogan & Hartson on 1994-08-15 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 26 510(k) clearances for Hogan & Hartson, from 1980-12-17 to 1998-01-23. As of 2026-09-10, FDA records show no recalls naming K942627.