FDA 510(k) Application Details - K954913

Device Classification Name Wire, Guide, Catheter

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510(K) Number K954913
Device Name Wire, Guide, Catheter
Applicant CARDIOMETRICS, INC.
645 CLYDE AVE.
MOUNTAIN VIEW, CA US
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Contact SUSAN E OSBORNE-NORIEGA
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Regulation Number 870.1330

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Classification Product Code DQX
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Date Received 10/03/1995
Decision Date 11/07/1995
Decision SE - Substantially Equivalent
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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