FDA 510(k) Applications Submitted by AVENT AMERICA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K051413 05/31/2005 ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100 AVENT AMERICA, INC.
K052047 07/29/2005 ISIS IQ UNO HANDHELD ELECTRONIC BREAST PUMP, MODEL 101 AVENT AMERICA, INC.


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