Radius Manual Whwwlchairs (Cobra, Viper, Swing, Olympia, and Mobil Models)

K951560 is the FDA 510(k) clearance record for RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS), a class I device, cleared for Radius Intl., Inc. on 1995-04-17 under FDA product code IOR (Wheelchair, Mechanical). FDA's definition for product code IOR reads: "A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position”...". FDA records list 5 510(k) clearances for Radius Intl., Inc., from 1995-02-01 to 1998-01-23. As of 2026-09-10, FDA records show no recalls naming K951560.