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FDA 510(k) Applications Submitted by HARRY PLATT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072385
08/24/2007
HEARTEVENT, MODEL AT
DIAGNOSTIC DEVICES PTY LTD
K030218
01/21/2003
PER, MODEL MEMO
MEDICAL MONITORS PTY., LTD.
K010751
03/13/2001
BPFONE, MODEL UA 767IT
MEDICAL MONITORS PTY LIMITED
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