FDA 510(k) Application Details - K930787

Device Classification Name Wire, Guide, Catheter

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510(K) Number K930787
Device Name Wire, Guide, Catheter
Applicant ADVANCED SURGICAL, INC.
305 COLLEGE RD. EAST
PRINCETON, NJ US
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Contact ANGELIQUE ANDERSON
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Regulation Number 870.1330

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Classification Product Code DQX
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Date Received 02/16/1993
Decision Date 07/09/1993
Decision SK - Substantially Equivalent - Kit
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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