
Neometrics, Inc.
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MODIFICATION TO VASCUPUNCTURE PICC GUIDEWIRE is an FDA 510(k)-cleared medical device (K043398) 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 February 28, 2005. Regulation: 8.