FDA 510(k) Application Details - K925381

Device Classification Name Wire, Guide, Catheter

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510(K) Number K925381
Device Name Wire, Guide, Catheter
Applicant ADVANCED CARDIOVASCULAR SYSTEMS, INC.
3200 LAKESIDE DR.
P.O. BOX 58167
SANTA CLARA, CA US
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Contact SARA TOYLOY
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Regulation Number 870.1330

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Classification Product Code DQX
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Date Received 10/23/1992
Decision Date 02/12/1993
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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