
AbbVie , Inc.
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AbbVie PEG is an FDA 510(k)-cleared medical device (K142793) manufactured by AbbVie , Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 13, 2015. Regulation: 8.