FDA 510(k), K944957, TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500
FDA 510(k), K944957, TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500
Device Name: TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500
Manufacturer:
Device Classification Name: Electrode, Pacemaker, Temporary
Regulation Number: 870.3680
Classification Product Code: LDF
Date Received: 10/07/1994
Decision Date: 07/14/1995
Regulation Medical Specialty: Cardiovascular
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