FDA 510(k) Applications Submitted by LORNE S CHARNBERG

FDA 510(k) Number Submission Date Device Name Applicant
K991007 03/26/1999 K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60 KATECHO, INC.
K981737 05/18/1998 K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60 KATECHO, INC.


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