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FDA 510(k) Applications Submitted by PAUL PHILLIPS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K151576
06/11/2015
Neon EEG
Incereb Ltd
K082312
08/13/2008
PRIME ECG SYSTEM (WITH ENHANCED DIAGNOSTIC ALGORITHM)
HEARTSCAPE TECHNOLOGIES LTD
K142709
09/22/2014
samaritan PAD 450P
HEARTSINE TECHNOLOGIES, INC.
K103631
12/13/2010
SLEEPMINDER BREATHING FREQUENCY INDICATOR
BIANCAMED LIMITED
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