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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