FDA 510(k) Application Details - K042493

Device Classification Name Computer, Diagnostic, Programmable

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510(K) Number K042493
Device Name Computer, Diagnostic, Programmable
Applicant ENDOCARDIAL SOLUTIONS, INC.
1350 ENERGY LN., SUITE 110
ST. PAUL, MN 55108 US
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Contact KAREN J MCKELVEY
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Regulation Number 870.1425

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Classification Product Code DQK
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Date Received 09/14/2004
Decision Date 10/15/2004
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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