FDA 510(k) Applications Submitted by EDWARD R KIMMELMAN

FDA 510(k) Number Submission Date Device Name Applicant
K974733 12/18/1997 BOEHRINGER MANNHEIM DIRECT LDL - CHOLESTEROL BOEHRINGER MANNHEIM CORP.
K974825 12/24/1997 BOEHRINGER MANNHEIM C.F.A.S. - HDL/LDL-C-PLUS BOEHRINGER MANNHEIM CORP.
K974826 12/24/1997 BM PRECIPATH(R) HDL/LDL-C CONTROL BOEHRINGER MANNHEIM CORP.


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