FDA 510(k) Applications Submitted by PULSE METRIC, INC.

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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