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FDA 510(k) Applications Submitted by ROBERT DUFFY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012498
08/03/2001
DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEM
PULSE METRIC, INC.
K013358
10/10/2001
DYNAPULSE 5000A MINI ABP BLOOD PRESSURE MONITORING SYSTEM
PULSE METRIC, INC.
K013478
10/19/2001
DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM
PULSE METRIC, INC.
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