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FDA 510(k) Application Details - K033245
Device Classification Name
Ligator, Esophageal
More FDA Info for this Device
510(K) Number
K033245
Device Name
Ligator, Esophageal
Applicant
C.R. BARD, INC.
129 CONCORD RD., BLDG. #3
BILLERICA, MA 01821 US
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Contact
MICHAEL A PATZ
Other 510(k) Applications for this Contact
Regulation Number
876.4400
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Classification Product Code
MND
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/07/2003
Decision Date
11/06/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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