MILENIA PAP IRMA CATALOG #: MKPA1, X

MILENIA PAP IRMA CATALOG #: MKPA1, X is an FDA 510(k)-cleared medical device (K902937) manufactured by Diagnostic Products Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 20, 1990. Regulation: 8.