Ellman Vapor-Vac II

K944558 is the FDA 510(k) clearance record for ELLMAN VAPOR-VAC II, a class II device, cleared for North American Technical Services Corp. on 1995-04-28 under FDA product code GEX (Powered Laser Surgical Instrument). FDA's definition for product code GEX reads: "A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue...". FDA records list 9 510(k) clearances for North American Technical Services Corp., from 1992-09-10 to 1998-06-22. As of 2026-09-10, FDA records show no recalls naming K944558.