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FDA 510(k) Applications Submitted by KAI HANSJURGENS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980892
03/09/1998
HAKOMED ELECDT / PRO ELEDT SERIES
ALIVE, INC.
K980958
03/16/1998
HAKOMED ELECDT/VACUPULLS
ALIVE, INC.
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