CATHETER, INTRAVASCULAR (ARGYLE IV SK)

CATHETER, INTRAVASCULAR (ARGYLE IV SK) is an FDA 510(k)-cleared medical device (K760760) manufactured by Sherwood Medical Industries. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 8, 1976. Regulation: 8.