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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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