FDA 510(k) Applications Submitted by EXTERNAL COUNTERPULSATION LAB

FDA 510(k) Number Submission Date Device Name Applicant
K012141 07/10/2001 AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE EXTERNAL COUNTERPULSATION LAB
K021340 04/26/2002 AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE EXTERNAL COUNTERPULSATION LAB


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