FDA 510(k) Applications Submitted by LAWRENCE DYER

FDA 510(k) Number Submission Date Device Name Applicant
K071347 05/14/2007 VAX-D GENESIS G2 SYSTEM VAX-D MEDICAL TECHNOLOGIES LLC
K053503 12/16/2005 VAX-D GENESIS SYSTEM (THERAPEUTIC TABLE) VAX-D MEDICAL TECHNOLOGIES USA, L.C.


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