FDA 510(k) Application Details - K050561

Device Classification Name Computer, Diagnostic, Programmable

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510(K) Number K050561
Device Name Computer, Diagnostic, Programmable
Applicant MEDCON LTD.
POB 6718
EFRAT 90435 IL
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Contact ELI M ORBACH
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Regulation Number 870.1425

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Classification Product Code DQK
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Date Received 03/03/2005
Decision Date 05/04/2005
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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