VASCUPUNCTURE PICC GUIDEWIRE

VASCUPUNCTURE PICC GUIDEWIRE is an FDA 510(k)-cleared medical device (K031652) manufactured by Neometrics, Inc.. 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 29, 2003. Regulation: 8.