Phx Technologies Corp.,hook Electrode, 5Mm

K934281 is the FDA 510(k) clearance record for PHX TECHNOLOGIES CORP.,HOOK ELECTRODE, 5MM, a class II device, cleared for Phx Technologies Corp. on 1994-02-25 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 49 510(k) clearances for Phx Technologies Corp., from 1993-11-18 to 1998-01-09. As of 2026-09-10, FDA records show no recalls naming K934281.