FDA 510(k) Application Details - K012678

Device Classification Name Catheter, Recording, Electrode, Reprocessed

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510(K) Number K012678
Device Name Catheter, Recording, Electrode, Reprocessed
Applicant STERILMED, INC.
11400 73RD AVE. NORTH
MAPLE GROVE, MN 55369 US
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Contact PATICK FLEISCHHACKER
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Regulation Number 870.1220

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Classification Product Code NLH
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Date Received 08/14/2001
Decision Date 08/14/2002
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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