Arthro-Flo Irrigation System Modification

K935617 is the FDA 510(k) clearance record for ARTHRO-FLO IRRIGATION SYSTEM MODIFICATION, a class II device, cleared for Davol Inc., Sub. C. R. Bard, Inc. on 1994-09-16 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 24 510(k) clearances for DAVOL INC., SUB. C.R. BARD, INC., from 1994-05-17 to 2010-07-15. As of 2026-09-10, FDA records show no recalls naming K935617.