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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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