FDA 510(k) Application Details - K854912

Device Classification Name Wire, Guide, Catheter

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510(K) Number K854912
Device Name Wire, Guide, Catheter
Applicant ANGIOMED U.S., INC.
4081 EAST LA PALMA AVE.,
SUITE E
ANAHEIM, CA US
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Contact RICHARD P MOHR
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Regulation Number 870.1330

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Classification Product Code DQX
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Date Received 12/09/1985
Decision Date 04/16/1986
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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