FDA 510(k) Applications Submitted by JENNIFER LAINE

FDA 510(k) Number Submission Date Device Name Applicant
K091787 06/17/2009 MODEL 6000 TWO PARAMETER BEDSIDE MONITOR IVY BIOMEDICAL SYSTEMS, INC.
K062943 09/28/2006 POLYSMITH SLEEP SYSTEM, MODEL NTI5498 NEUROTRONICS, INC.


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