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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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