Vapr 2.3 Mm Side Effect Electrode for Use with Vapr System

K992876 is the FDA 510(k) clearance record for VAPR 2.3 MM SIDE EFFECT ELECTRODE FOR USE WITH VAPR SYSTEM, a class II device, cleared for Mitek Products on 1999-09-24 under FDA product code HRX (Arthroscope). FDA's definition for product code HRX 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 30 510(k) clearances for Mitek Products, from 1996-10-01 to 2002-03-14. As of 2026-09-10, FDA records show no recalls naming K992876.