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FDA 510(k) Applications Submitted by PULSE BIOMEDICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100813
03/23/2010
QRS CARD S-T SEGMENT ANALYSIS PATIENT MONITORING SYSTEM MODEL: QRS CARD USB
PULSE BIOMEDICAL, INC.
K972255
06/17/1997
PULSE BIOMEDICAL INC, QRS CARD S-T SEGMENT ANALYSIS MONITORING SYSTEM
PULSE BIOMEDICAL, INC.
K042799
10/08/2004
QRS-CARD CARDIOLOGY SUITE
PULSE BIOMEDICAL, INC.
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