0.22 MICRON FINAL FILTER WITH EXTENSION TUBE

0.22 MICRON FINAL FILTER WITH EXTENSION TUBE is an FDA 510(k)-cleared medical device (K935601) manufactured by Puritas Health Care, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 20, 1994. Regulation: 8.