MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENT

MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENT is an FDA 510(k)-cleared medical device (K875327) manufactured by Schneider-Shilley (Usa). This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 24, 1988. Regulation: 8.