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FDA 510(k) Application Details - K062832

Device Classification Name Instrument, Biopsy

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510(K) Number K062832
Device Name Instrument, Biopsy
Applicant C.R. BARD, INC.
P.O. BOX 1740
1625 W. 3RD STREET
TEMPE, AZ US
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Contact GLENN NORTON
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Regulation Number 876.1075

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Classification Product Code KNW
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Date Received 09/21/2006
Decision Date 10/20/2006
Decision SE - Substantially Equivalent
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review N



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