BUFFALO FILTER VIROSAFE HRF- #VSHRFO1

BUFFALO FILTER VIROSAFE HRF- #VSHRFO1 is an FDA 510(k)-cleared medical device (K983333) manufactured by Buffalo Filter Co., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 10, 1999. Regulation: 8.