FDA 510(k) Applications Submitted by ALEXANDER B HENDERSON SR.

FDA 510(k) Number Submission Date Device Name Applicant
K082861 09/29/2008 AMCO REPLACEMENT BATTERY FOR POWERHEART AED, NON-RECHARGEABLE, MODEL 2L561; G3, NON-RECHARGABLE, MODEL 7L561 AMCO INTERNATIONAL MANUFACTURING & DESIGN, INC.


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