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FDA 510(k) Application Details - K960176
Device Classification Name
Tube, Double Lumen For Intestinal Decompression And/Or Intubation
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510(K) Number
K960176
Device Name
Tube, Double Lumen For Intestinal Decompression And/Or Intubation
Applicant
C.R. BARD, INC.
100 SOCKANOSSETT CROSSROAD
CANSTON, RI 02920 US
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Contact
ROBIN DRAGO
Other 510(k) Applications for this Contact
Regulation Number
876.5980
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Classification Product Code
FEG
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More FDA Info for this Product Code
Date Received
01/16/1996
Decision Date
07/24/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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