FDA 510(k) Application Details - K910720

Device Classification Name Kit, Needle, Biopsy

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510(K) Number K910720
Device Name Kit, Needle, Biopsy
Applicant C.R. BARD, INC.
8195 INDUSTRIAL BLVD.
COVINGTON, GA US
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Contact DONNA J WILSON
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Regulation Number 876.1075

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Classification Product Code FCG
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Date Received 02/20/1991
Decision Date 06/10/1991
Decision SE - Substantially Equivalent
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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