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FDA 510(k) Application Details - K953008
Device Classification Name
Tube, Feeding
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510(K) Number
K953008
Device Name
Tube, Feeding
Applicant
MARQUETTE MEDICAL, INC.
1114 BENFIELD BLVD., SUITE K
MILLERSVILLE, MD 21108 US
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Contact
EARL D MARQUETTE, JR.
Other 510(k) Applications for this Contact
Regulation Number
876.5980
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Classification Product Code
FPD
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More FDA Info for this Product Code
Date Received
06/28/1995
Decision Date
01/11/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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