POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER

POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER is an FDA 510(k)-cleared medical device (K990276) manufactured by Porous Media Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 1999. Regulation: 8.