FDA 510(k) Application Details - K890404

Device Classification Name Wire, Guide, Catheter

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510(K) Number K890404
Device Name Wire, Guide, Catheter
Applicant C.R. BARD, INC.
1200 TECHNOLOGY PARK DR.
P.O. BOX 7025
BILLERICA, MA US
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Contact JANICE T PIASECKI
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Regulation Number 870.1330

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Classification Product Code DQX
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Date Received 01/24/1989
Decision Date 08/17/1989
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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